CA2556564A1

CA2556564A1 - Spinal facet joint implant

Info

Publication number: CA2556564A1
Application number: CA002556564A
Authority: CA
Inventors: Robert W. Hoy; Alan Chervitz; T. Wade Fallin; Daniel J. Triplett; Daniel F. Justin
Original assignee: Facet Solutions, Inc.; Robert W. Hoy; Alan Chervitz; T. Wade Fallin; Daniel J. Triplett; Daniel F. Justin
Current assignee: Facet Solutions Inc
Priority date: 2004-02-17
Filing date: 2005-02-17
Publication date: 2005-09-01
Also published as: US20090030461A1; US20050131538A1; JP4959345B2; US8911475B2; US20140058449A1; US9339394B2; WO2005079426A2; US20050131537A1; US20170007419A1; US8926700B2; EP1715820A4; US20050131409A1; US8579941B2; US8419770B2; US8449579B2; US7588590B2; AU2005214933A1; WO2005079426A3; US7753937B2; US9579217B2

Abstract

Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra.

Description

SPINAL FACET JOINT IMPLANT
Background of the Invention [0001] Field of the Invention [0002] The present invention relates to surgical devices and methods to ~~uidc:
instruments that prepare the surface of bones and other tissues for implants that replace a damaged, diseased, or otherwise painful spinal facet joint.

[0003] Description of Related Art [0004] Traumatic, inflammatory, metabolic, and degenerative disorders of the spine can produce debilitating pain that can have severe socioeconomic and psychological eliects.
One of the most common surgical interventions today is arthrodesis, or spine fusion, of one or more motion segments, with approximately 300,000 procedures performed annually in the United States. Clinical success varies considerably, depending upon technique and indications, and consideration must be given to the concomitant risks and complications. For example, Tsantrizos and Nibu have shown that spine fusion decreases function by limiting the range of motion for patients in flexion, extension, rotation, and lateral bending.
Furthermore, I~hoo and Nagata have shown that spine fusion creates increased stresses and, therefore, accelerated degeneration of adjacent non-fused motion segments.
Additionally.
pseudoarthrosis, as a result of an incomplete or ineffective fusion, may reduce or even eliminate the desired pain relief for the patient. Finally, the fusion device, whether artificial or biological, may migrate out of the fusion site.

[0005] Recently, several attempts have been made to recreate the naaual biomechanics of the spine by use of an artificial disc. Artificial discs provide for articulation between vertebral bodies to recreate the full range of motion allowed by the elastic properties of the natural intervertebral disc that directly connects two opposed vertebral bodies.

[0006] However, the artificial discs proposed to date do not fully address the mechanics of motion of the spinal column. In addition to the intervertebral disc, posterior elements called the facet joints help to support axial,~torsional and shear loads that act on the spinal column. Furthermore, the facet joints are diarthroidal joints that provide both 511CIlll~.r articulation and load transmission features. The effects of their absence as a result of facetectomy was observed by Goh to produce significant decreases in the stiffness at' the spinal column in all planes of motion: flexion and extension, lateral bending, alld rotation.

Furthermore, contraindications for artificial discs include arthritic facet joints, absent facet joints, severe facet joint tropism or otherwise deformed facet joints, as noted by Lemaire.

[0007] U. S. Patent Number Re. 36,758 to Fitz discloses an artificial facet joint where the inferior facet, the mating superior facet, or both, are resurfaced.

[0008] U. S. Patent Number 6,132,464 to Martin discloses a spinal facet ,joint prosthesis that is supported on the posterior arch of the vertebra. Extending from this support structure are inferior and/or superior blades that replace the cartilage at the facet joint. The Martin prosthesis generally preserves existing bony stmctures and therefore does not address pathologies that affect the bone of the facets in addition to affecting the associated cartilage Furthermore, the Martin invention requires a mating condition between the prosthesis and the posterior arch (also known as the lamina) that is a thin base of curved bone that carries all four facets and the spinous process. Since the posterior arch is a very complex and highly variable anatomic surface, it would be very difficult to design a prosthesis that provides reproducible positioning to correctly locate the cartilage-replacing blades for the facet joints.

(0009] Another approach to surgical intervention for spinal facets is provided in W09848717A1 to Villaret. While Villaret teaches the replacement of spine facets, the replacement is interlocked in a manner to immobilize the joint.

[0010] It would therefore be an improvement in the art to provide a vertebral facea replacement device and method that provides a relatively high degree of mobility in the joint, while effectively removing the source of arthritic, traumatic, or other disease mediated pain with a minimum of patient discomfort.
Summary of the Invention [0011] In order to overcome the shortcomings of the prior art, the present invention provides a vertebral facet replacement device and method that replaces a bony portion of the facets so as to remove the source of arthritic, traumatic, or other disease mediated pain. Fact joint replacement in conjunction with artificial disc replacements represent a holistic solution to recreating a fully functional motion segment that is compromised due to disease or traltllla.
Together, facet joint and disc replacement can eliminate all sources of pain, return lull function and range of motion, and completely restore the natural biomechanics of the spinal column. Additionally, degenerative or traumatized facet joints may be replaced in the absence of disc replacement when the natural intervertebral disc is unaffected by the disease or trauma.

[0012] Accordingly, in certain embodiments, the present invention provides an artificial vertebral facet that replaces the cartilage and a portion of the bone of a facet.
Furthermore, the invention may provide a method for preparing a vertebra for the installation of an artificial vertebral facet, a method for replacing a spinal facet, and possibly, a total vertebral facet joint replacement.

[0013] The present invention may provide numerous advantages over the prioz-a~~t.
One advantage may be that the quality of attachment of the prosthesis is improved. The present invention may provide a precise press fit into bones, as opposed to relying c,n prosthetic surfaces mating with highly complex and variable extemlal surfaces of the vertebra, such' as the posterior arch or facet. Another advantage may be that the optional porous coating is placed into interior bone spaces where porous coatings have proven to achieve bone ingrowth for excellent long term fixation strength. This ability to achieve bone ingrowth is uncertain for the plzor art devices that engage the external bone surfaces of the vertebra. Yet another advantage may lie in the removal of the facet bone structure; where the facet bone is involved in the disease pathology or the trauma that compromised the articular or cartilaginous surface of the facet, resection provides a means for ensuring that all pain associated with the disease or trauma is removed.

[0014] The above, and other features and advantages of the present invention, will become apparent from the following description, which is to be read in conjunction with the accompanying drawings.
Brief Description of the Drawings [0015] Fig. 1 is a perspective view of a portion of the spine;

[0016] Fig. 2 is a lateral view of a facet joint reconstructed in accordance with the present invention;

[0017] Fig. 3 is a dorsal view of the facet joint shown in Fig. 2;

[0018] Fig. 4 is a perspective view of the implanted Ieft inferior facet prostheses shown in Figs. 2 and 3;

(0019] Fig. 5 is a perspective view of the left inferior facet proStheSlS
ShoWI1 111 I~i<~s.
2 and 3;

[0020] Fig. 6 is a cranial view of the implanted left superior facet prosthesis shown in Figs. 2 and 3;

[0021] Fig. 7 is a perspective view of the left superior facet prosthesis shown in Fi~~s.
2 and 3;

[0022] Fig. 8 is a perspective view of an alternative implanted left inferior facet prosthesis;

[0023] Fig. 9 is a perspective view of an alternative left inferior facet prosthesis, [0024] Fig. 10 is a lateral view of an alternative reconstructed facet joint;

[0025] Fig. 11 is a dorsal view of an alternative reconstructed facet joint;

[0026] Fig. 12 is a perspective view of the implanted left inferior facet prosthesis shown in Figs. 10 and 11;

[0027] Fig. 13 is a perspective view of the alternative left inferior facet prosthesis shown in Figs. 10 and 11;

[0028] Fig. 14 is a cranial view of the alternative implanted left superior facet prosthesis shown in Figs. 10 and 11;

[0029] Fig. 15 is a perspective view of the alternative left superior facet prosthesis shown in Figs. 10 and 11;

[0030] Fig. 16 is a perspective view of an alternative bearing surface for the superior facet prosthesis shown in Fig. 15;

[0031] Fig. 17 is a dorsal view of a single intact vertebra;

[0032] Fig. 18 is a lateral view of the same intact vertebra shown in Fig. 17;

[0033] Fig. 19 is a dorsal view of the same vertebra of Fig. 17 and Fig. 18, with a portion of the superior facet resected and a portion of the inferior facet resected;

[0034] Fig. 20 is a lateral view of the resected vertebra shown in Fig. 19;

[0035] Fig. 21 is a dorsal view of the same resected vertebra shown in Fig. 18 allCl Fig. 19 with a fixation element placed through the first superior resection surface and into the pedicle bone;

[0036] Fig. 22 is a dorsal view showing the resected veuebra, the fixation element.
and a superior facet prosthesis;

[0037] Fig. 23 is a dorsal view of the vertebra and the implant of Fig. 23 and also showing the addition of an inferior facet prosthesis;

[0038] Fig. 24 is a dorsal view of the implant and vertebra of Fig. 23 and also showing the addition of an enlarged head that has the shape of a locking nut;

[0039] Fig. 25 is a perspective view of a vertebra with an assembled implant comprising a fixation element, superior facet prosthesis, and a locking nut;

[0040] Fig. 26 is a perspective, cross-sectioned view of the same vertebra and implant of Fig. 25 with a cross section aligned with the axis of the fixation element;

[0041] Fig. 27 is a cranial, cross-sectioned view of the vertebra and implant of Fi~~.
25, with the section plane positioned as in Fig. 26;

[0042] Fig. 28 is a side view of embodiments A, B, C, D, E, and F of the fixation element, a cross-sectional view of each of embodiments A, B, C, D, E, and F, and a side vie:w~
of the enlarged head in the shape of a locking nut;

[0043] Fig. 28A is a side view of embodiments G, H, I, J, K, and L of the fixation element with attached enlarged heads, and a cross-sectional view of each of embodiments G, H, I, J, K, and L;

[0044] Fig. 29 is a perspective view of a radially expanding fixation element in its unexpended state;

[0045] Fig. 30 is a side view and a bottom view of (i) an expanded radially expandini~
fixation element and (ii) an unexpended radially expanding fixation element;

[0046] Fig. 31 is a perspective cross-sectional view of a vertebra and a facet implant showing a cross-pin torsionally and axially securing the fixation element;

[0047] Fig. 32 is a dorsal view of a spinal section showing a top, middle, and bottom vertebra with unilateral facet replacements on the right side of the spine section, both between the top and middle vertebra, and between the middle and bottom vertebra;
[004] Fig. 33 is a dorsal view of a spine section showing a superior hemiarthroplasty facet replacement between the top and the middle vertebra and unilateral replacement between the middle and the bottom vertebra;
[0049] Fig. 34 is a dorsal view of a spinal section showing an inferior facet hemiarthroplasty replacement between the top and the middle vertebra and a unilateral replacement on the right side between the middle and the bottom vertebra;
[0050] Fig. 35 is a dorsal view of a spinal section showing a unilateral replacement between the top and middle vertebrae on the right side, and an inferior facet hemianlwoplastv replacement between the middle and bottom vertebrae on the same side;
[0051] Fig. 36 is a dorsal view of a spinal section showing a unilateral replacement between the top and middle vertebrae on the right side and a superior facet hemiarthroplasty replacement on the right side between the middle and bottom vertebrae on the same side;
[0052] Fig. 37 is a spinal section of two vertebrae showing one inferior facet of the top vertebra and the adjoining superior facet of the bottom vertebra replaced by an articulating facet implant;

[0053] Fig. 38 is a perspective view of a curved superior facet prosthesis;
[0054] Fig. 39 is a perspective view of a superior facet prosthesis with a bone ingrowth surface;
[0055] Fig. 40 is a perspective view of an inferior facet prosthesis;
[0056] Fig. 41 is a perspective view of an inferior facet prosthesis with a bone ingrowth surface;
[0057] Fig. 42 is an exploded, perspective view illustrating the addition of a loclcint~
washer to the construction of the implant shown in Fig. 25;
[0058] Fig. 43 is a perspective view illustrating the implant of Fig. 25 with a loclcin~~
washer fully installed;
[0059] Fig. 44 is a perspective view of the locking washer shown in Fig. 42;
[0060] Fig. 45 is a perspective view of superior and inferior facet prostheses held against a vertebra by flexible fixation elements;
[0061] Fig. 46 is a dorsal view of a bilateral inferior implant;
[0062] Fig. 47 is perspective view of a vertebra with an alternative embodiment oi° a superior facet prosthesis fixed to the bone by one embodiment of a fixation element;
[0063] Fig. 48 is a perspective, cross-sectional view of the embodiment of the superior facet prosthesis and fixation element of Fig. 47 showing the semispherical shape ol°
the resection and the approximately similarly semispherical shape of the apposition side of the superior facet prosthesis, as well as an angled resection and corresponding angled flat on the apposition side of the superior facet prosthesis in combination with the semispherical resection;
[0064] Fig. 49 is a perspective view of the resected vertebra without the superior facet prosthesis attached to the vertebra, in which the fixation element is installed in the vertebra;
[0065] Fig. 50 is a perspective view of the resected veuebra with the superior facet prosthesis attached to the vertebra, with the fixation element installed in the vertebra, but without the locking fastener shown in Fig. 47;
[0066] Fig. 51 is a top view of the superior facet prosthesis showing the semispherical shape of the bone apposition side in combination with the angled flat on the bone apposition side;
[0067] Fig. 52 is a rear view of the superior facet prosthesis showing the semispherical nut engaging surface on the top of the area that is design to comiect to the fixation element and the locking nut, or the inferior prosthesis and the fixation element;

[0068] Fig. 53A is a rear view and a perspective view of a plurality of superior faces prostheses of a kit;
[0069] Fig. S3B is a top view of an inferior facet prosthesis according to one embodiment of the invention;
[0070] Fig. S3C is a side view of the inferior facet prosthesis of Fig. S3B;
[0071] Fig. 53D is a perspective view of a plurality of inferior facet prostheses ol' a lcit;
[0072] Fig. 53E is a perspective view showing how a superior facet prosthesis and an inferior facet prosthesis may fit together;
[0073] Fig. S3F is a dorsal view of an LS superior facet prosthesis and an L4 inferior facet prosthesis fit on adjacent vertebrae to articulate against each other;
[0074] Fig. S3G is a posteriolateral view of the implants and vertebrae shown in Firs.
53F;
[0075] Fig. S3H is a posteriolateral view showing a cross-section along a first plane cut through the articulation of the implants of Fig. S3F;
[0076] Fig. 53I is a cephalad view showing a cross-section along a second plane cut through the articulation of the implants shown in Fig. S3F;
[0077] Fig. S4 is a dorsal view of a bilateral inferior facet prosthesis system and a superior facet prosthesis in situ;
[0078] Fig. 55 is a perspective view of the bilateral inferior facet prosthesis system and the superior facet prosthesis of Fig. S4;
[0079] Fig. S6 is a lateral view of the bilateral inferior facet prosthesis system and superior facet prosthesis in situ;
[0080] Fig. S7 is a cranial view of the bilateral inferior implant system in situ;
[0081] Fig. 58 is a bottom view of the bilateral inferior facet prosthesis system in situ, [0082] Fig. S9 is rear view of the bilateral inferior facet prosthesis system in isolation;
(0083] Fig. 60 is a top view of the bilateral inferior facet prosthesis system in isolation;
[0084] Fig. 61 is a bottom view of the bilateral inferior facet prosthesis system in isolation;
[0085] Fig. 62 is a perspective view of the right inferior prosthesis;
[0086] Fig. 63 is a perspective view of various ball-shaped members of inferior prostheses, the ball-shaped members having differing surface features, particularly circumferential grooves, longitudinal grooves, and knurling;

[0087] Fig. 64 is an end view of the ball-shaped members of Fig. 63; and [0088] Fig. 65 is a dorsal view of the bilateral inferior facet prosthesis system, in which castle nuts are attached to the left and right fixation elements.
Detailed Description of the Drawings [0089] Referring now to Fig. 1, there is shown a perspective view of a superior vertebra 1 and an inferior vertebra 3, with an intervertebral disc 2 located in between. The superior vertebra 1 has superior facets 43, inferior facets 6, a posterior arch (or lamina) 3 and a spinous process 46. The inferior vertebra 3 has superior facets 7, inferior facets 44, a posterior arch (or lamina) 36 and a spinous process 45. Each of the vertebrae l, 3 also has a pair of pedicles 11.
[0090] Referring now to Fig. 2, in a lateral view, the left inferior facet 6 of the superior vertebra 1 shown in Fig. 1 has been resected and an inferior facet prosthesis 4 has been attached to the superior vertebra 1. Similarly, the left superior facet 7 of the inferior vertebra 3 has been resected and a superior facet prosthesis 5 has been attached to the inferior vertebra 3.
[0091] Fig. 3 illustrates a dorsal view of the elements shown in Fig. 2. It can be appreciated that inferior facet prosthesis 4 replicates the natural anatomy when compared to the contralateral inferior facet 6 of vertebra 1. Similarly, it can be appreciated that superior facet prosthesis 5 replicates the natural anatomy when compared to the contralateral superior facet 7 of vertebra 3. Neither the inferior facet prosthesis 4 nor the superior facet prosthesis rests on the lamina 35.
[0092] Turning now to Fig. 4, a perspective view of the superior vertebra 1 with implanted inferior facet prosthesis 4 is provided. A bone resection on the left side ol' the superior vertebra l, shown as a resection 31, has removed the natural inferior facet 6 at the bony junction between the inferior facet 6 and the lamina 35. In this manner, any bone pam associated with a disease, such as osteoarthritis, or trauma of the left inferior facet 6 will br eliminated as the involved bony tissue has been osteotomized.
[0093] Fig. 5 illustrates a perspective view of the inferior facet prosthesis 4.
surface 8 replicates the natural articular surface of the replaced inferior facet 6. A post o provides a mechanism that can be used to affix the inferior facet prosthesis 4 to the superior vertebra 1. The post 9 is implanted into the interior bone space of the left pedicle 11 on the superior vertebra 1 and may or may not extend into the vertebral body of superior vertebra 1 to provide additional stability.
(0094] Fig. 6 illustrates a cranial view of the inferior vertebra 3 with the implanted superior facet prosthesis 5. A resection surface 32 represents the bony junction between the natural superior facet 7 and the lamina 36.
[0095] Fig. 7 illustrates a perspective view of the superior facet prosthesis ~. f~
surface 38 replicates the natural articular surface of the replaced superior facet 7. The post 37 provides a mechanism usable to affix the superior facet prosthesis 5 to tha inferior ve~~tebra 3.
The post 37 is implanted into the interior bone space of the left pedicle 11 (Fig. 6j on the inferior vertebra 3 and may or may not extend into the vertebral body of the inferior vertebra 3 to provide additional stability.
[0096] When the total facet joint is replaced, as shown in Figs. 2 and 3, then the surface 8 (Fig. 5) articulates agailist the surface 38 (Fig. 7) to recreate the natural biomechanics of the spine motion segment made up of the superior vertebra l, the inferior vertebra 3, and the intervertebral disc 2. Neither the inferior facet prosthesis 4 nor the superior facet prosthesis 5 rests on the lamina 35 or the lamina 36, respectively.
[0097] Fig. 8 illustrates a perspective view of an alternative inferior facet prosthesis that may be implanted into the interior bone space of the lamina 35 of the superior vertebra 1. The interior bone space is accessed from the resection 31.
[0098] Fig. 9 shows a perspective view of the alternative inferior facet prosthesis I U.
including a fin 13 that extends into the interior bone space of the 35. A
surface 12 replicates the natural articular surface of the replaced facet.
[0099] The surfaces of the post 9 (Fig. 5), the post 37 (Fig. 7), and the rin 13 (Fig. 9) may or may not include porous coatings to facilitate bone ingrowth to enhance the long-term i_ixation of the implant. Furthermore, such porous coatings may or may not include osteoinductive or osteoconductive substances to further enhance bone remodeling into the porous coating. In this application, the term "implant" refers to any natural or man-made, fabricated or unfabricated device or group of devices that may be added to a human spine.
An implant may include one or more prostheses, one or more fixation devices, and/or other components.
[00100] Referring now to Fig. 10, there is shown a lateral view of a superior vertebra 14 and an inferior vertebra 16, with an intervertebral disc 15 located in between. The Icl't inferior facet of the superior vertebra 14 has been resected and an inferior facet prosthesis I
has been attached to superior vertebra 14 via a screw fastener 17. Similarly, the left superior facet of the inferior vertebra 16 has been resected and a superior facet prosthesis 19 has been attached to vertebra 16 via a screw fastener 17.
[00101] Fig. 11 illustrates a dorsal view of the elements of Fig. 10. It can be appreciated that inferior facet prosthesis 18 replicates the natural anatomy when compared to the contralateral inferior facet 22 of the superior vertebra 14. Similarly, it can be appreciated that superior facet prosthesis 19 replicates the natural anatomy when compared to the contralateral superior facet 21 of the inferior vertebra 16. Neither the inferior facet prosthesis 18 nor the superior facet prosthesis 19 rests on the lamina of the corresponding vertebra I4 car 16.
[00102] Turning now to Fig. 12, there is provided a perspective view of the superior vertebra 14 with the implanted inferior facet prosthesis 18. A resection 34 has removed thr natural inferior facet at the bony junction between the inferior facet and the adjoining lamina.
In this manner, any bone pain associated with a disease, such as osteoarthritis, or trauma oi~
the natural inferior facet 22 will be eliminated inasmuch as the involved bony tissue has been osteotomized.
[00103] Fig. 13 illustrates a perspective view of the inferior facet prosthesis 18. A
surface 23 replicates the natural articular surface of the replaced facet. A
flange 25 contacts the pedicle 11 (Fig. 12) and a hole 24 receives the screw fastener 17 to attach the interior facet prosthesis 18 to the superior vertebra 14.
[00104] Fig. 14 illustrates a cranial view of the inferior vertebra 16 with the implanted superior facet prosthesis 19. A resection surface 33 represents the bony junction between the natural superior facet 21 (Fig. 11) and the corresponding lamina.
[00105] Fig. 15 illustrates a perspective view of the superior facet prosthesis 19. n surface 27 replicates the natural articular surface of the replaced facet. A
flange 39 contacts the pedicle 11 (Fig. 14) and hole 26 receives a screw fastener 17 to attach the superior Facet prosthesis 19 to the inferior vertebra 16.
[00106] Fig. 16 provides a perspective view of an alternative superior facet prosthesis 40 with a bearing surface 41 that mounts to substrate 42. The bearing surface 41 is n biocompatible polymeric material, such as ultra high molecular weight polyethylene.
Alternatively, the bearing surface can be ceramic, such as zirconia or alumina. The substrate is a biocompatible metal alloy, such as an alloy of titanium, cobalt, and/or iron.
[00107] The bearing surface 41 may be formed separately from the remainder of the superior facet prosthesis 40, so that the bearing surface 41 and the remainder Dorm components that can be assembled as needed. A lcit of differently-sized prostheses may include multiple bearing sLwfaces like the bearing surface 41 that may have different thicknesses, articulating surface shapes, material selections, and the lilee.
Such a lcit may also include other differently-sized components designed such that some subset of the components can be selected and assembled together to provide a prosthesis having the desired dimensions.
Prosthesis kits will be shown and described in greater detail subsequently.
[00108] Referring to Fig. 17 and Fig. 18, a single intact vertebra 100 is shown. Fig. 17 is a dorsal view of the vertebra 100. Fig. 18 is a lateral view of the same vertebra IOCI.
Similar to the two vertebrae 1, 3 shown in the portion of the spine illustrated in Fi~~s. I
through 3, the vertebra 100 has posterior anatomy comprising left and right superior facets ~13 on the superior, or top side in this view of the dorsal vertebra 100, left and right inferior facets 6 on the inferior or bottom side of the posterior vertebra 100, left and right transverse processes 105 extending laterally from the posterior portion of vertebra 100, and left and right pedicles 11. Each of the superior facets 43 has a superior articulating surface 145. The posterior portion of vertebra 100 also has a posterior arch (or lamina) 35, and a spinous process 46 that protrudes from the lamina 35 posteriorly, out of the page in Fig. 17 and to the left in Fig. 18. In Fig. 17, the bony structure of the superior facets 43 and the inferior facets 6 are intact, as it would be presented in a vertebra without significant tissue degeneration or remodeling resulting from facet joint disease. Although the vertebra 100 is shown in Fib. 17 as a generally structurally healthy and intact vertebra, if the vertebra 100 were a diseased vertebra, the vertebra could exhibit signs of facet joint disease.
[00109] Consequently, structural pathology related to facet joint disease would likely be visible. For example, the left superior facet 43 and the right superior facet 43 0l' the vertebra 100 are symmetrical in Fig. 17 and Fig. 18. But in the case of a vertebra 100 with only one diseased joint, the facet on the diseased side would likely be showing patholo~~ical signs of disease such as tissue degeneration or inflammation resulting in an asymmetrical structural comparison between the two facets.
[00110] Also, in more extreme cases the facet disease could progress to a state in which the articular process of the facet is eroded or inflamed resulting 111 atlatOtlltC
morphology that is unique to the pathology of a particular facet joint of an individual patient.
This could present unusual facet morphology that could be different from what is shown in Figs. 17 and 18.
[00111] Furthermore, the facet disease could eventually disable the biomechanics o (' a patient such that the facet joint is essentially non-articulating and immobile. In this case. one superior facet of a first vertebra could essentially be fused to one inferior facet of a second vertebra. Since the structural pathology of the diseased facet is variable, a surgeon may determine that the best bone apposition surface or foundation for securing a facet implant is a resected bone surface.
[00112] Referring to Fig. 19 and Fig. 20 which are dorsal and lateral views of the saint:
vertebra shown in Fig. 17 and Fig. 18 after a portion of the right superzor facet 43 and a portion of the right inferior facet 6 have been resected. The removal of a portion of the superior facet 43 by resection results in a superior facet resection 111. In the resection shown in Fig. 19 and Fig. 20, the superior resection 111 has two resulting faces, a first resection surface 112 and a second resection surface 113. Likewise, the inferior facet resectioi-1 results in an inferior facet resection surface 121.
[00113] Tissue removal tools (not shown) such as a bone burr, rasp, reamer, 111111, sam.
younger, osteotome or similar tools designed to cut and remove bone tissue can be used to create these resection surfaces. The surgeon uses anatomic landmarlcs such as the pedicle I 1 or transverse process 105 to align the tissue removal tools in such a way as to remove the portion of the facet necessary to provide a superior resection 111 that serves as a bone apposition surface or foundation to eventually support a superior facet prosthesis 300. as shown in Fig. 22. The left superior facet 43 is shown intact in both Fig. 19 and Fig. 20. but a portion of the right superior facet 43 is resected resulting in the first resection surface 112 and the adjacent second resection surface 113 (Fig. 19). The shape of the superior resection 1 1 I
will vary in accordance with the structure of the tissue removal tool. In the embodiment shown in Fig. 19 and Fig. 20, the first resection surface 112 and the second resection surlacc 113 are on approximately perpendicular planes. However, the geometry of the resection surfaces is a function of the patient anatomy, the pathology of the diseased tissue. the technique of the surgeon, and other factors such as the type of tissue removal tools used to prepare the resection. In general, the first resection surface 112 will be formed in such a way that it will serve as a foundation to support the superior facet prosthesis 300 (Fig. 22). The second resection surface 113 or other additional resection surfaces may or relay Ilot be present.
[00114] Fig. 19 and Fig. 20 also show that a portion of the inferior facet 6 is resected by tissue removal instruments resulting in an inferior resection surface 121.
Such resection is preferably effected so that resection is confined to the tissue of the inferior facet 6 and docs not extend into the tissue of the posterior arch (or lamina) 35. In Figs. 19 and 20. the leti inferior facet 6 is intact, while a portion of the right inferior facet 6 is resected resulting in ten;
inferior resection surface 121 on the right side. The bone suwounding the inferior resection surface 121 is contoured by tissue removal tools in a shape designed to cradle and support an inferior facet prosthesis 400 (Fig. 23) on the medial side such that when the inferior facet prosthesis 400 is loaded on the lateral side it compresses against and is supported vy the inferior resection surface 121.
[00115] Alternatively, the inferior facet 6 can be resected, and inferior facet prosthesis 400 sized and shaped, so that inferior facet prosthesis 400 does not engage the inferior resection suuace 121.
[00116] Fig. 21 is a dorsal view of the vertebra 100 with a fixation element 200 placed through the superior resection 111 and into the bone of the pedicle 11 to receive the superior facet prosthesis 300 (Fig. 22). The fixation element 200 is aligned and placed into the pedicle 11, similar to how other pedicle screws for posterior stabilization involved with vertebrae fusion are placed in the pedicle 11. In one method, a long guide wire (not shown). with a diameter sized to fit freely into a cannulation 211 (as also shown in Fig. 26 and Fig. 27) in the fixation element 200, is placed through the first resection surface 112 and into the bone of the pedicle 11. The alignment of the long guide wire can be confiuned by x-ray.
The fixation element 200 is then guided over the guide wire and driven into the vertebra 100 by a driver (not shown) engaged with a drive feature 212 (Fig. 21) on a proximal post 230 of the fixation element 200. The fixation element 200 is driven into the vertebra 100 until a comiection feature 213 (e.g., a screw thread) is just above the first resection surface 112. This connection feature 213 is eventually used to secure the superior facet prosthesis 300 to the vertebra 100.
[00117] In a second method for guiding the fixation element 200 into the pedicle 1 I . a long guide wire (not shown), with a diameter sized to fit freely into a cammlation in a bone preparation instrument (not shown) such as a tap, drill, broach or reamer, is placed tllrou~~h the first resection surface 112 and into the bone of the pedicle 11. The alignment of the lon'.:
guide wire can be confirmed by x-ray. The bone preparation instrument is then guided over the guide wire and driven into the bone of the pedicle 11 to prepare a cavity for the fixation element 200. The guide wire and bone preparation instrument are then removed and the fixation element 200 is guided into the prepared cavity in the pedicle 11 by a driver ( not shown) engaged with the drive feature 212 on the proximal post 230 of the fixation element 200. Like in the first method, the fixation element 200 is duiven into the vertebra until a connection feature 213 (e.g., a screw thread) is just above the first resection surface 11~'.
This connection feature 213 is eventually used to secure the superior facet prosthesis 300 to the vertebra 100.

[00118] In yet a third method of placing the fixation element 200 in the pedicle, ihc:
surgeon aligns the fixation element 200 with anatomic landmarks and simply drives the fixation element 200 through the first resected surface 112 and into the pedicle 11. As v,ith the first and second methods, the fixation element 200 is driven into the vertebra 100 until a connection feature 213 (e.g., a screw thread) is just above the first superior resection surface 112.
[00119] In Fig. 22, a dorsal view illustrates a superior facet prosthesis 300 placed around the fixation element 200. The superior facet prosthesis 300 has a facet articulatin~~
component 320 that articulates against the inferior facet articulating surface of the vertebra above it. The facet articulating component 320 is preferably foixned in the general shape of a blade or wing ear. The superior facet prosthesis 300 also has a bone apposition stwface 3??
that has been placed on the first resection surface 112 and an opening 324 in a flange 323 that smTOUnds the fixation element 200. The superior facet articulating component 320 has an articulating surface 321 generally adjacent to the flange 323 that is oriented in a direction that faces approximately the same direction that the original anatomic superior articulatinr~
surface 145 faced prior to resection.
[00120] This orientation of the articulating surface 321 allows the superior facet prosthesis 300 to function as either a hemiarthroplasty implant and articulate against a natural anatomic inferior facet 6 or act as a portion of a unilateral prosthesis and articulate against an inferior facet prosthesis 400 on the vertebra superior (cephalad) to it. No portion of superior facet prosthesis 300 rests on the lamina of the vertebra 100. In this application, a "unilateral prosthesis" is a prosthesis in which both facets of only one of the facet joints between adjacent vertebrae are replaced by prostheses. A "hemiarthroplasty" is a type of artlwoplasty in which one side of an articulating joint surface is replaced with an artificial implant.
[00121] Fig. 23 is a dorsal view showing the addition of the inferior facet prosthesis 400 to the construct described in Fig. 22. The inferior facet prosthesis 400 generally has a shape similar to a longitudinal rod that is curved to match the contour of the inferior resection 121 (Figs. 19 and 20). The inferior facet prosthesis 400 has an opening 4I0 tluough its superior end 420 that is shaped to surround the portion of the fixation element 200 that protrudes from the first resection surface 112. In Fig. 23, the inferior facet prosthesis 400 is placed over the superior facet prosthesis 300. However, the order of the placement of the prostheses 300, 400 can be reversed such that the inferior prosthesis 400 is placed on the fixation element 200 first, followed by the superior prosthesis 300. When only the inferior facet 6 or the superior facet 43 is being replaced, only the appropriate (superior or inferior) facet prosthesis 300 or 400 is placed on the fixation element 200 without the other (inferior or superior) facet prosthesis 300 or 400.
[00122] Because the various components of the implant are modular. many combinations of configurations and implant size, structure and shapes are feasible. For example, in a patient with unusual anatomy, the inferior facet prosthesis 400 may need to be larger than expected to confomn to a particularly unusual or exceptionally large morphology of the inferior resection surface 121, and the superior facet prosthesis 300 may need to have an unusual angle to its articulating surface 321 to conform to particular anatomic constraints.
If this is the case, the modularity of the system allows for the surgeon to assemble an implant specifically designed to match the patient's anatomic structures during the sur~~e~y. This flexibility of a modular implant design allows the implant manufacturer to accommodate a large variation in anatomic structures with a limited selection of implant component size.
shapes, and material types.
[00123] The modularity of the implant design also allows different components of the implant to be fabricated from different materials. Traditionally, bone fixation implants such as the fixation element 200 are fabricated from biocompatible metals or alloys that provide sufficient strength and fatigue properties, such as cobalt chrome alloys, titanium and titanium alloys, and stainless steels. However, the fixation element 200 may be fabricated from ceramics, polymers, or biological materials such as allograft bone, composites, or other biocompatible structural materials. Likewise the superior facet prosthesis 300 and the inferior facet prosthesis 400 may. be fabricated from metals, alloys, ceramics, polymers, biological materials, composites, or other biocompatible structural materials.
[00124] In Fig. 24, a dorsal view illustrates the addition of an enlarged head 500 to the fixation element 200. The enlarged head 500 is tightened down to force the prostheses 3011.
400 against the bone to stabilize them. The enlarged head 500 shown in Fig. 24 has o hexagonal geometry on its external surface that is shaped to accept a driver (not shown) that is used to force an internal connection feature 520 (e.g., a screw thread) of the enlarged head 500 onto the connection feature 213 of the fixation element 200. In the case of the threaded embodiment of the connection feature 213, the enlarged head 500 is provided with a threaded connection feature 520 and is driven onto the fixation element 200 by turning the enlar~~ed head 500 and allowing the threads to drive all components of the implant between the enlarged head 500 and the first resection surface 112 against the bone at or near the resection surface 112.

[00125] Fig. 25 is a perspective posterior view of the assembly of the fixation element 200, the superior facet prosthesis 300, and the enlarged head 500. The enlarged head 500 has been placed on the first resection surface 112.
[00126] Fig. 26 is a perspective, cross-sectioned view of the same constmct ShoWll lIl Fig. 25. The superior facet prosthesis 300, the enlarged head 500, the fixation element ?0U.
and the vertebra 100 have been cut by a cross-sectioning plane 150 placed along an axis that passes through the center of the fixation element 200. The cross-section plane 150 is shown for visualization purposes to illustrate, using a cross-sectioned view, how the vertebra lO), fixation element 200, superior facet prosthesis 300 and the enlarged head 500 engage each other. In actual surgery, it is highly unlikely that a surgeon would make a cut as illustrated by°
the cross-section 150 shown in Fig. 26.
[00127] Fig. 27 is a cranial, section view of the vertebra 100 and the implant, wherein the cross-section plane 150 is oriented to face the viewer. In Fig. 27, the fixation element 20() is in the vertebra 100. The embodiment of the fixation element 200 in Fig. 27 comprises a, distal end 220 that is shaped to guide the fixation element 200 into bone tissue, a bone stabilizing portion 210 adjacent to the distal end, a shaft portion 240 adjacent to the bone stabilizing portion 210, a connection feature 213 adjacent to the shaft portion 240, and a drive feature 212.
[00128] The distal end 220 shown in Fig. 27 has a frusto-conical shape that allows the fixation element 200 to be driven or guided into the vertebra 100. The distal end 220 could be shaped in the form of a spade tip, trochar tip, or twist drill tip to assist in the guidance o1 the fixation element 200 in the vertebra 100. The fixation element 200 may also have a cutting flute (not shown) formed in the distal end 220 to help remove bone tlsSLle alld accommodate the guidance of the fixation element 200 in the vertebra 100. The Lone stabilizing portion 210 helps to secure the fixation element 200 to the vertebra 100. The bone stabilizing portion 210 can include various features designed to anchor into bone such as threads, ribs, grooves, slots, fins, barbs, splines, bone ingrowth surfaces, roughened surfaces, or any geometric feature that helps to engage the fixation element 200 with the bone tissue to help stabilize the fixation element 200. In Fig. 27, the bone stabilizing portion ? 10 has a unitary continuous bone thread 231. However, other types of tlweads such as multiple lead threads, variable pitched thread, non-uniform pitch thread, buttress thread, or other thread forms used on bone screws may be used. Because Fig. 27 is a cross-sectional view, the full length of the cannulation 211 is seen passing from the distal end 220 of the fixation element 200 to the proximal post 230 of the fixation element 200.

[00129] The drive feature 212 in the embodiment shown in Fig. 27 is an inteznal hex.
However, any shape of drive feature 212 that transmits the loads necessazy to drive the fixation element 200 into the vertebra 100 can be formed on the proximal post 330 of the fixation element 200. The depth of the drive feature 212 formed in the proximal post ?30 0l the fixation element 200 is seen in the cross-sectional view of Fig. 27. The drive feature ? 1?
may be an internal drive feature such as the hex socket shown in this embodiment, or an external drive feature with geometry on the periphery of the proximal post 230 of the fixation element 200 that engages with a corresponding internal drive feature on a driver tool (not shown). In this embodiment the depth of the drive feature 212 is slightly longer than its cross-section is wide. This depth can be adjusted based on the material properties of the fixafiion element 200 and the drive tool (not shown).
[00130] The fixation element 200 is fabricated from biocompatible base materials that provide the necessazy structural rigidity and strength. Examples of base materials that may be used in the construction of the fixation element 200 include titanium, titanium allow, cobalt-chrome alloys, stainless steel alloys, zirconium alloys, other biocompatible metal materials, biocompatible ceramics, biocompatible composites, and biocompatible polymers.
The fixation element 200 may also have surface materials formed on the base material that provide material properties specific to a particular poz-tion of the fixation element 200. For example, the bone stabilization portion 210 could be coated with materials that allow for improved bone ingrowth into the implant surface such as a hydroxylapatite, bioceramic.
Bioglass", or other calcium phosphate derived material. The tribological bearing properties of the material in the areas that the fixation element 200 interfaces with other artificial elements may be improved by applying surface hardening techniques to the material of the fixation element 200 in these areas. Surface hardening techniques known in the materials science and materials engineering ants such as anodizing, ion implantation, and other techniques could be applied to these isolated areas.
[00131] As mentioned previously, the connection feature 213 is formed on the portion of the fixation element 200 that protrudes from the first resection surface Il?. This connection feature 213 is designed to connect the enlarged head 500 to the fixation element 200. In the embodiment of the connection feature 213 shown in Fig. 21, threads 260 are can the exteznal surface of this proximal section of the fixation element 200.
These tlweads 26C1 engage with the threads of the inteznal connection feature 520 (Fig. 27) of the enlarged head 500. Although the connection feature 213 in this embodiment is threaded, other mechanical locking features (not shown) capable of loclting the fixation element 200 and the enlarged head 500 together, such as press fit, taper fit, bonding fit by cement or glue, interference Fit, expansion fit and mechanical interlocking flt such as a bayonet connection, can be used as the connection feature 213. A corresponding construction may then be used as connection feature 520 of the enlarged head 500.
[00132] Also shown in Fig. 27 is a cross-sectional view of the superior facet prosthesis 300. This embodiment of the superior facet prosthesis 300 has a flange 323 that has an opening 324 that receives the fixation element 200. In the assembled and nnplanted configuration of this embodiment, the flange 323 is positioned such that its bone apposition surface 322 makes contact with the first resection surface 112. Although not shown in thi:~
embodiment, other embodiments of the superior facet prosthesis 300 have structures (c.g., spikes) that protrude into the first resection surface 112 to help resist torsion and other anatomic loads. Protl~zding from the flange 323 at a given angle a, and a given distance ?e from the opening 324, is the articulating component 320. The articulating surface 321 of the facet articulating component 320 replicates the natural articular surface of the replaced facet.
Once the surgeon assesses the anatomy of the superior facet 43 that is being replaced, a particular superior facet prosthesis 300 is selected that has the angle a and the distance X that best fits the anatomy of the level of vertebra, the left or right side, and the size of the patient's anatomy being replaced. Thus a lcit containing various sizes and shapes of superior facet prostheses 300 is provided to the surgeon and the surgeon selects the superior facet prosthesis 300 that best suits the situation.
[00133] After the fixation element 200 and the superior facet prosthesis 3UC) are selected and placed, they are locked to the vertebra 100 by the enlarged head 500. As shown in Fig. 24, the enlarged head 500 in this embodiment has an internal connection featlwe ~?() and a hexagonal shaped extel~rlal drive feature 510 that is used to drive the enlarged head SOt) over the fixation element 200 and against the superior facet prosthesis 300.
The specific shape of the external drive feature 510 is dependent on the mating shape of the driver ( not shown).
[00134] Referring to Fig. 28, side and cross-sectional views illustrate six different embodiments of fixation elements, which are labeled A, B, C, D, E, and F. The figure shown a side view of each fixation element embodiment and a cross-sectional view ol' each embodiment to the light of the respective side view. To the left of the six embodiments is a representative enlarged head 500. Embodiment A is the threaded fixation element ?Ut~
embodiment shown in Figs. 26 and 27 and described above. Embodiments B
tln'Oll~~h E are various designs of fixation elements with non-circular cross-sections.
Embodiment I3 is n four rib cruciate design with four longitudinal fms 285 configured to resist torsion when the fixation element 200 is in the vertebra 100. Embodiment C is an oval shaped cross-section design that is wider in the first direction 286 than the second direction 287 to resist torsion. I l' the width in the first direction 286 is equal to the width in the second direction 287, the cross-section shape becomes more of a circle and bone stabilization portion 210 becomes more of a press-fit peg. Embodiment D is a square cross-section design with four approximately perpendicular sides 288. The corners 289 of the sides 288 help to resist torsion. Embodiment E is a triangular cross-section design with three sides 291 to resist torsion.
Embodiment F is an anchor-like design that is driven into the vertebra, with the wire arches or barbs 290 bein~~
compressed against the host bone and applying a radial expansion force so as to lock the structure to the bone.
[00135] Referring to Fig. 28A, side and cross-sectional views illustrate six more different embodiments of fixation elements, which are labeled G, H, I, J, K, and L. Fi~~. ?8A
shows a side view of each fixation element embodiment and a cross-sectional view of each embodiment to the right of the respective side view. Each embodiment has an attached or integrally formed enlarged head 500'. Embodiment G is similar to the threaded fixation element 200 embodiment shown in Figs. 10, 11, 12 and 24 and described above.
Embodiments H through K are various designs of fixation elements with non-circular cross-sections. Embodiment H is a four rib cruciate design with four longitudinal fins 28~
configured to resist torsion when the fixation element is in the vertebra 100.
Embodiment I is an oval shaped cross-section design that is wider in a first direction 286 than in a second direction 287 to resist torsion. If the width in the first direction 286 is equal to the width in the second direction 287, the cross-section shape becomes more of a circle and the bone stabilization portion 210 becomes more of a press-fit peg. Embodiment J is a square cross-section design with four approximately perpendicular sides 288. The comers 289 of the sides 288 help to resist torsion. Embodiment K is a triangular cross-section design with three sides 291 to resist torsion.
[00136] Embodiment L is an anchor-like design that is similar to Embodiment E
in Fi~~.
28, but with an attached or integrally foamed enlarged head 500'. As embodiment L is driven into the vertebra, wire arches or barbs 290 are compressed and apply radial expansion force against the wall of the prepared bone and into the pedicle 11, resulting in a locking anchor.
[00137] Fig. 29 is a perspective view of a radially expanding fixation element 60(1.
The radially expanding fixation element 600 comprises two main elements, an expansion sleeve 620 and a central element 610 that is inside of the expansion sleeve 620. The radially expanding fixation element 600 is placed into the vertebra 100 and then the central element 610 is drawn outward relative to the expansion sleeve 620 resulting in radial expansion ol~ the fixation element 600. This is shown in Fig. 30.
[00138] Referring to Fig. 30, side and bottom views illustrate the fixation element G00 of Fig. 29. As a proximal post 630 of the central element 610 is pulled axially alOll~r its longitudinal axis, and the expansion sleeve is held axially in the bone by compression 1-'it.
talons 621 on the expansion sleeve 620 are radially expanded outward by a mandrel 660 on the central element 610. The talons or fingers 621 provide both torsional and axial stability to the radially expanding fixation element 600. This provides a secure fixation element lt~r fixation of the remaining implant components. Furthemnore, expansion of the fixation element 600 may cause the fixation element 600 to center itself within the pedicle 11.
[00139] Fig. 31 is a perspective, cross-sectional view of a cross-pin element 7i)0 engaged with the fixation element 200 to help secure the fixation element 200 both torsionally and axially. The cross-pin element 700 is columnar in shape having a distal enci 710, a midsection 730 (with a length along its longitudinal axis that is longer than its transverse cross-sectional width), and a proximal post 720. The distal end 710 is shaped to penetrate through bone tissue and into a cross hole 280 formed in the fixation element 20().
Instrumentation (not shown) is used to align the cross-pin element 700 with the cross-hole 280 via fixation of the instrumentation to the drive feature 212 or the cammlation 211 on thr-fixation element 200 and alignment of the direction of insertion of the cross-pin element 70() with the cross-hole 280. Once the cross-pin element 700 is in place in the bone and tlll'OLlL~l7 the fixation element 200, the torsional and axial stability of the fixation element ?()() is improved.
[00140] The various embodiments of the fixation element 200 described above and shown in Fig. 28 through Fig. 31 function in conjunction with the enlarged head 500 to held the inferior facet prosthesis 400 and/or the superior facet prosthesis 300 to their respective resection surfaces 112, 113, and/or 121. Various combinations of this modular implant will be described below and shown in Figs. 32 through 37. Although these figures illustrate the use of the fixation element 200 and the enlarged head 500 as the mechanism for securin4x the prostheses 300, 400 to the vertebra 100, other clamping devices such as the screw fastener 17 (Fig. 10) may be used to mount the prostheses 300, 400 to the bone. For example, the screw prostheses 17 shown in Figs. 10 through 12 may pass through either the opening 324 ( Fi~~.
22) in the superior facet prosthesis 300 or the opening 410 (Fig. 23) in the inferior facet prosthesis 400 or through both of these openings 324, 410. The head of the screw fastener 17 acts as the securing mechanism by pressing the inferior facet prosthesis 400 and the superior facet prosthesis 300 against their respective resection surfaces 112, 113, and/or 121.
[00141] Figs. 32 through 37 demonstrate different combinations of assemblies of facet replacement prostheses. The basic components of the prosthesis are the fixation element 2U(~, the superior facet prosthesis 300, the inferior facet prosthesis 400, and the enlarged head SUU.
However, as described above, a screw fastener 17 can replace the fixation element 20U anti the enlarged head 500.
[00142] Referring to Fig. 32, a dorsal view illustrates three sequential layers of vertebrae. A top vertebra 101 is above a middle vertebra 102, and the middle vertebra 102 is above a bottom vertebra 103. Portions of some of the facets on the right side of the vertebrae are replaced by prostheses. With regard to the facet joint between the top vertebra 101 anti the middle vertebra 102, an inferior facet prosthesis 401 is articulating against a superior facet prosthesis 302 to form an artificial unilateral joint. The inferior facet of the middle vertebra 102 is replaced by an infet~ior facet prosthesis 402 and the superior facet of the bottom vertebra 103 is replaced by superior facet prosthesis 303. Thus, a second unilateral prosthetic joint is formed that is also on the right side and is located at the level between the middle vertebra 102 and the bottom vertebra 103. Fig. 32 demonstrates the difference m shape of the inferior facet prosthesis 401 that is implanted around the fixation element ?() 1 without a superior facet prosthesis 300 and an inferior facet prosthesis 402 that is implanted around a fixation element 202 and over a superior facet prosthesis 302. The opening 410 (not visible) of the inferior facet prosthesis 401 on the top vertebra 101 in this assembly is offset more laterally than the opening 410 (not visible) in the inferior facet prosthesis 402 for the middle vertebra 102. This is because the fixation element 201 is implanted more laterally on the top vertebra 101 to preserve more of the superior facet since it is not replaced by a prosthesis at this level.
[00143] RefetTing to Fig. 33, a dorsal view illustrates the top vertebra 101 in intact form, without resection of the facets. Portions of both the superior and inferior facets on the right side of the middle vertebra 102 are replaced by a superior facet prosthesis 302 and an inferior facet prosthesis 402. Only the right superior facet of the bottom vertebra 103 is replaced (i.e., by a superior facet prosthesis 303) in Fig. 33. Thus, a hemiartlwoplasty replacement has been performed on the right facet joint between the top vertebra 101 and the middle vertebra 102 and a unilateral replacement has been performed between the middle vertebra 102 and the bottom vertebra 103. The assembly shown in Fig. 33 demonstrates how the superior facet prosthesis 302 can articulate against the natural inferior facet 6 and the superior facet prosthesis 303 can articulate against the inferior facet prosthesis 402.
[00144] Fig. 34 is a dorsal view illustrating how the inferior facet prosthesis 40I can articulate against the natural superior facet 43, or the inferior facet prosthesis 402 can articulate against the superior facet prosthesis 303. The right facet joint between the top vertebra 101 and the middle vertebra 102 is a hemiarthroplasty replacement with the interior facet replaced by the inferior facet prosthesis 401. The right facet joint between the middle veuebra 102 and the bottom vertebra 103 is a unilateral replacement with the inferior facet replaced by the inferior facet prosthesis 402 and the superior facet of the bottom vertebra 103 replaced by the superior facet prosthesis 303.
[00145] Referring to Fig. 35, a dorsal view shows another example of how the supericsr facet prosthesis 303 can articulate against the natural inferior facet 6 or the superior tacei prosthesis 302 can articulate against the inferior facet prosthesis 401. In this assembly of tl2e implant, the right side between the top vertebra 101 and the middle vertebra 102 is a unilateral replacement and the right side between the middle vertebra 102 and the bOtt0111 vertebra 103 is a hemiarthroplasty replacement.
[00146] RefeiTing to Fig. 36, a dorsal view shows another example of how the inferior facet prosthesis 402 can articulate against the natural superior facet 43, or the inferior facet prosthesis 401 can articulate against the superior facet prosthesis 302. The right facet joint between the top vertebra 101 and the middle vertebra 102 is a unilateral replacement with the inferior facet of the top vertebra 101 replaced by the inferior facet prosthesis 401 and the superior facet of the middle vertebra 102 replaced by the superior facet prosthesis 302. The right facet joint between the middle vertebra I02 and the bottom vertebra 103 is a hemiarthroplasty replacement with the inferior facet replaced by the inferior facet prosthesis 402.
[00147] Referring to Fig. 37, a dorsal view illustrates only one level, that between the middle vertebra 102 and the bottom vertebra 103, being replaced on the right side. The right facet joint between the middle vertebra I02 and the bottom vertebra 103 is a unilateral replacement with the inferior facet of the middle vertebra 102 replaced by the inferior facet prosthesis 402 and the superior facet of the bottom vertebra 103 replaced by the superior facet prosthesis 303.
[00148] Fig. 38 and Fig. 39 show two embodiments of the superior facet prosthesis. In Fig. 38, a perspective view illustrates an embodiment in which a curved superior f~crt prosthesis 305 with a curved articulating component 330 has a curved articulating surl°ace 331. This curved articulating surface 331 allows for a more distributed contact load between an inferior facet prosthesis, such as the inferior facet prosthesis 400 of Fig. 23, and the curved articulating surface 331. This allows slightly more flexibility in the position that the surgeon places the curved supeuor facet prosthesis 305 than the superior facet prosthesis 3()(~
previously described. The articulating surface 321 of the superior facet prosthesis 3()() previously described is relatively flat. The articulating surface 331 of the curved superior facet prosthesis 305 is curved. Since the bearing portion of the inferior facet prosthesis 4UU is columnar, the two prosthesis can be aligned on a slight mismatch and make more of an anatomic contact if the articulated surface is curved as in Fig. 38.
[00149] Refen-ing to Fig. 39 a perspective view illustrates a bone ingrowth feature 39U
on a superior facet prosthesis 306. The bone ingrowth feature 390 can be any surface that allows bone to grow into the implant between the first resection surface 112 of the vertebra 100 and the apposition surface 322 of the implant. Examples of bone ingrowth feat<wes 3~)(~
include porous coating of beads or meshes, electrochemically etched shapes and porous pads pressed onto the implant surface made from tantalum, titanium, cobalt chrome alloys andior other biocompatible material such as hydroxylapatite or calcium phosphate ceramics.
[00150] Referring to Fig. 40, a perspective view shows the inferior facet prostlleSls 400, which is formed in the general shape of a finger or talon. More particularly, the inferior facet prosthesis 400 is formed with a flange 420 on its superior side shaped to fit between the enlarged head 500 and either the superior facet prosthesis 300 or the first resection surtacc 112. The flange 420 has an opening 410 that is dimensioned to allow the inferior facet prosthesis 400 to fit over the proximal post 230 of the fixation element 200 and around the shaft portion 240 of the fixation element 200. The inferior facet prosthesis 40U also has an inferior portion 450 on the opposite side of the flange 420 that has a bone apposition side 44U
that is shaped to contact the surface of the inferior facet resection sunace 121 (Fig. 19) and a joint articulation side 430 that is shaped to articulate against a natural or prosthetic superior facet.
[00151] Referring to Fig. 41, a perspective view shows an inferior facet prosthesis 4G() also formed in the general shape of a finger or talon. The inferior facet prosthesis 46() is formed with a superior end 420 having an opening 410 that is dimensioned and Shaped to accept the fixation element 200. The inferior facet prosthesis 460 is generally columnar in shape, having a curved length designed to conform to the prepared anatomy of the vertebra 100. The inferior facet prosthesis 460 of Fig. 41 has an inferior portion 470, which is shown opposite the superior end 420, and slightly medially offset from the superior end 42U. This medial offset of the opening 410 relative to the inferior portion 470 allows the inferior iacct prosthesis 400 to be anchored to the bone by the fixation element 200 and secured to the bone by the enlarged head 500, or the superior facet prosthesis 300 in combination with the enlarged head 500, at an anatomical position that allows optimal bone fixation. The inferior facet prosthesis 460 of Fig. 41 has a bone ingrowth surface 441 and a joint articulating side 430 on its inferior end 470. In this embodiment, the bone ingrowth surface 441 is a textured structure that permits bone cells to grow into the implant surface. The shape of the bone ingrowth surface 441 can be a uniform textured surface as shown in Fig. 41, or Call be a non-uniform randomized structure such as a open cell foam structure, a porous beaded structure, a wire mesh structure, an electrochemical etched structure, or other bone ingrowth stmct<wes known in the design of orthopedic implants. The bone ingrowth surface 441 is shaped to mate with the inferior resected bone surface 121 shown in Fig. 19 and Fig. 20.
[00152] Fig. 42 shows an exploded, perspective view of the vertebra 100 with the superior facet prosthesis 300 installed. An additional locking washer 800 is used to assist in stabilizing the attachment of the superior facet prosthesis 300 to the first resection surface 112. The construction of the implant assembly shown in Fig. 42 is similar to that of the assembly shown in Fig. 25 with the addition of the locking washer 800 that is placed over and around the proximal post 230 of the fixation element 200.
[00153] Referring to Fig. 43, a perspective view shows the same implant of Fi~~. 4?
with the enlarged head 500 locked onto the fixation element 200 and pushing the locking washer 800 against the superior facet prosthesis 300 and into the bone tissue.
This added bone penetration of the locking washer 800 helps to fix the superior prosthesis 300 SL1CI1 that the entire assembly is more mechanically stable with respect to the vertebra 100.
[00154] Fig. 43 shows a further step in the assembly of the implant constmct described in Fig. 42. In Fig. 43, the locking washer 800 is secured over the fixation element 200 and into the bone tissue by the enlarged head 500. Although this embodiment of the loclcin'~
washer 800 is only shown with the superior facet prosthesis 300, the locking washer 800 can alternatively be used to mechanically secure the inferior facet prosthesis 400. or the combination of the inferior facet prosthesis 400 and the superior facet prosthesis 300. In the embodiment of the locking washer 800 shown in Fig. 42 and Fig. 43, the locking washer 8tU
is placed over the superior facet prosthesis 300. However, the locking washer 800 may he placed under the superior facet prosthesis 300, under the inferior facet prosthesis 400 and the superior facet prosthesis 300, or between the superior facet prosthesis 300 and the inferior facet prosthesis 400 to stabilize the implant construct.

[00155] Fig. 44 shows a perspective view of the locking washer 800. The loclcin~,~
washer 800 has a body 805 with an opening 810 that is dimensioned to fit over the proximal post 230 of the fixation element 200. The locking washer 800 also has an anti-rotation feature 820 that mates with either the superior facet prosthesis 300 or the inferior 1°acet prosthesis 400 or a combination of both the inferior facet prosthesis 400 and the superior facet prosthesis 400. The anti-rotation feature 820 shown in this embodiment is a tlat surface, however, any feature that would rotationally constrain the locking washer 8(?0 to the other components of the implant (such as a tab, groove, taper or other geometric shape) can be foirned on the locking washer 800 as an anti-rotation feature. The locking washer 8(m also has prongs 830 that pass into the bone tissue of the vertebra 100 to help stabilize the implant construct. The prongs 830 in this embodiment of the locking washer 80() arc elongated protrusions that taper to a tissue penetration tip 840. The prongs have sidewalk 850 that provide a surface to resist torsion once the locking washer 800 penetrates the bone tissue. The prongs 830 may also be simple spikes that are either synunetrical or asymmetrical in cross-section that protrude from the locking washer body 805.
The shape and length of the locking washer prongs 830 are dependent on how the locking washer 800 is used. The prongs 830 of the locking washer 800 that holds only one of the inferior facet prosthesis 400 or the superior facet prosthesis 300 to the vertebra 100 may be shorter than prongs of a locking washer that holds both the inferior facet prosthesis 400 and the superior facet prosthesis 300 to the vertebra 100.
[00156] Fig. 45 shows a perspective view of the superior facet prosthesis 300 anti inferior facet prosthesis 400 held to the vertebra 100 by an adjunctive flexible fixation element 900 and a secondary flexible fixation element 910. These flexible fixation elements 900 and/or 910 may be made from such constructs as suture, braided cable, wire, ribbon.
and/or other constructs that have longer lengths than cross-sections and withstand larger loads in tension than in compression. The flexible fixation elements 900 and/or 910 may be manufactured from biocompatible metals, alloys such as cobalt clwome alloys, titanium alloys, stainless steel alloys, polymers, bioabsorbable materials, composites, or other materials that are biocompatible and can be formed into a flexible element stmcturc 9()() and/or 910 such as those shown in Fig. 45. The adjunctive flexible element 900 shown in Fig. 45 is shown attached to and securing the elongated head 500. A flexible element attachment portion 580 (e.g., including an opening) mates the flexible element 900 to the elongated head. However, the adjunctive flexible fixation element 900 may alternatively or additionally be attached to the fixation element 200, the superior facet prosthesis 30(). the inferior facet prosthesis 400 or any combination of the above listed elements.
A llexiblc fixation attachment portion 480 (e.g., including an opening) in the inferior facet prosthesis 400 allows the secondary flexible fixation element 910 to secure the inferior facet prostheses 400 to the vertebra 100. The flexible fixation elements 900 and/or 910 may be secured to the vertebra 100 by physically wrapping them around anatomic features such as the posterior arch 35, the spinous process 46, transverse process 105, or a combination of these anatomic features. The flexible element 900 and the secondary flexible element 910 may also be secured to the vertebra 100 by bone anchors such as anchors designed to anchor flexible fixation elements (such as suture, not shown) to bone. Suture anchors such as threaded suture anchors, barbed suture anchors, toggle suture anchors or any other means of anchoring a flexible fixation element to bone may be used to anchor the flexible fixation element 90(J
and/or the secondary flexible fixation element 910 to the vertebra 100.
[00157] Fig. 46 is a dorsal view of a bilateral inferior facet prosthesis 100(). 'f h~
bilateral inferior facet prosthesis 1000 is a one-piece inferior facet prosthesis that has both a right inferior side 1040 and a left inferior side 1020 connected by a stabilizing bar 101 tJ.
Both the right inferior side 1040 and the left inferior side 1020 are designed to fix to the top vertebra 101 at the respective inferior resection surface 121 (Fig. 19) and at the first resection surface 112. The bilateral inferior facet prosthesis 1000 allows replacement of both the left and the right inferior facets. In this embodiment, the bilateral inferior facet prosthesis 1000 is placed over the left and right fixation elements 200 which extend into the bone of the toh vertebra 101. In the embodiment shown in Fig. 46, the right inferior side 1040 is articulatin~~
against the right superior facet prosthesis 300 attached to the bottom vertebra 102. Also in this embodiment, the left inferior side 1020 is articulating against the left natural superior facet 43 of the bottom vertebra 102. The stabilizing bar 1010 of the bilateral inferior prosthesis 1000 is designed to stabilize the left side 1020 and the right side 1040 so that they are secure.
[00158] Fig. 47 illustrates a perspective view of a superior facet prosthesis 1 lOJ
coupled to the vertebra 3. The superior facet prosthesis 1100 has a bone apposition surl-acc (not shown) that has been placed on a first resection surface 1112 and an opening (not shown ) in a flange 1116 that surrounds a fixation element 1110, and coupled thereto by a loclcin<~
fastener such as a castle nut 1114 or the like. The superior facet prosthesis 1100 has a superior facet articulating component 1120 with an articulating surface 1122 generally adjacent to the flange 1116. The articulating surface 1122 is oriented in a direction that faces approximately the same direction that the original anatomic superior articulating surlacc faced prior to resection. This orientation of the auiculating surface 1122 allows the superior facet prosthesis 1100 to function as either a hemianhroplasty implant by articulating against a natural anatomic inferior facet 6 or as a unilateral prosthesis by articulating against an inferior facet prosthesis on the vertebra superior (cephalad) to it, such as the inferior facet prostheses ~l shown in Fig. 5, the inferior facet prostheses 10 shown in Figs. 8 and 9, and the inferior facet prosthesis 400 shown in Fig. 40, as well as those described below.
[00159] The facet articulating component 1120 is preferably formed in the general shape of a blade or wing ear, wherein the articulating surface 1122 has a concave shape. In the embodiment shown, the articulating surface 1122 curves from an orientation generally perpendicular to the flange 1116 towards an orientation generally parallel to the flan ~~e 1 1 l O
from a distal end 1124 thereof to a proximal end 1126 thereof.
[00160] The concave shape of the articulating surface 1122 provides more tolerance for a miss-match with the natural anatomic inferior facet 6 or with the inferior facet prosthesis 4 on the vertebra superior to it. Functionally, the clearance between the concave shape of the articulating surface 1122 and the adjacent inferior facet 6 or inferior facet prosthesis 4 increases as the patient bends forward (flexion) and decreases as the patient bends backward (extension). Thus in flexion the patient has more facet movement allowin~~
for more torsion (twisting) and lateral bending (side to side movement) than in a neutral stance. As the patient extends, the articulating members are more constrained in torsion and lateral bending. This mimics the natural anatomic constraints of the spinal facets.
[00161] Fig. 48 is a perspective view of the same constmct shown in Fig. 47, but with the implants and the vertebra 3 cut by a cross-sectioning plane 1130 placed along an axis that passes through the center of the fixation element 1110. The cross-section plane 1130 shown cutting through the vertebra 3 and the implant of Fig. 47 is shown for visualization pmposcs to illustrate, using a cross-sectioned view, how the vertebra 3, fixation element 1110, and superior facet prosthesis 1100 engage each other.
[00162] The fixation element 1110 provides a mechanism that affixes the superior facet prosthesis 1100 to vertebra 3. Fixation element 1110 is implanted into the interior bone space of the left pedicle 11 (Fig. 6) on the vertebra 3 and may or may not extend into the vertebral body of vertebra 3 to provide additional stability. The fixation element 1110 can take the form of a screw (as shown), or any of the devices shown in Figs. 28-30. The fixation element 1110 has a drive feature 1140, which is an internal hex in the embodiment shown Ill Fig. 48. However, any shape of drive feature that transmits the loads necessary to drive the fixation element 1110 into the vertebra 3 can be formed on a proximal post 1142 of the fixation element 1110.
[00163] The depth of the drive feature 1140 formed in the proximal post 1142 of the fixation element 1110 is seen in the cross-sectional view of Fig. 48. The drive feature I 140 may be an internal drive feature such as the hex socket shown in this embodiment, or an external drive feature with geometry on the periphery of the proximal post 1142 of the fixation element 1110 that engages with a corresponding internal drive feature on a driver tool (not shown). The flange 1116 of the superior facet prosthesis 1100 is secured to the fixation element 1110 by the castle nut 1114 or the like.
[00164] The flange 1116 of the superior facet prosthesis 1100 includes a couplin~~
portion 1144 having a generally semispherical bone engaging surface 1150 on the apposition side of the superior facet prosthesis 1100 that engages a corresponding semispherical resection 1146 in the bone bed of the pedicle of vertebra 3. The term "semispherical" relates to a surface that includes some sectoual portion of a sphere, which may be less than a hemisphere. A semispherical surface may be concave or convex. A surface that i, semispherical or generally semispherical may have some deviations from a precise semispherical shape.
[00165] The semispherical resection 1146 may be said to be "inversely shaped"
with respect to the coupling portion because the semispherical resection 1146 has a generally concave surface that matches the generally convex surface of the coupling portion 1 144.
Although the coupling portion 1144 and the semispherical resection 1146 are semispherical in the embodiment of Figs. 47 and 48, in alternative embodiments, they may have a variety oi~
other matched shapes, including three-dimensional parabolas, ellipsoids, and other regularly or irregularly curved or flat-sided shapes. Furthermore, although the coupling portion I I 44 is convex and the semispherical resection 1146 is concave in the embodiment of Figs. 47 and 48, in alternative embodiments, the shapes may be reversed so that a coupling portion is concave and a resection is convex.
(00166] In the embodiment of Figs. 47 and 48, the coupling portion 1144 is integrally formed with the articulating surface 1122 of the superior facet articulating component 112(t.
The coupling portion 1144 may be said to be "attached to" the articulating surface 112'_' because in this application, the term "attached" is used broadly to include parts that are integrally formed with each other as well as parts that are formed separately and subsequently coupled together.

[00167] The semispherical resection 1146 in the bone bed allows for less transverse process to be resected (vs. a flat bone bed resection). The semipherical resection 1146 in the bone bed also allows for more stable support of the superior facet prosthesis 1100, than does a flat bone bed resection, as the superior facet prosthesis 1100 is polyaxially supported in such a way as to resist any shear forces applied between the semispherical resection 1146 and the coupling portion 1144. In this application, "polyaxial" refers to a linear or angular force or motion acting with respect to at least two perpendicular axes. The coupling portion I 14-1 may seat directly against the semispherical resection 1146. In this application, an item that "seats directly against" another is positioned to abut the other item so that surfaces of the two items are in contact with each other.
[00168] The coupling portion 1144 has a fixation element receiving aperture 1148 that can be made slightly larger than a circumferential diameter of the fixation element 1110 taken in a direction perpendicular to a longitudinal axis thereof to provide accurate polyaxial seating of the implant 1100 in relation to the resected bone bed and fixation element 1110. as well as to provide increased tolerance for miss-match. An implant engaging end 1 I 54 of the castle nut 1114 (or other fastener) also has a semispherical shape for engaging a semispherical nut engaging side of the coupling portion 1144 of the superior facet prosthesis 1100 at the final position of the superior facet prosthesis 1100.
[00169] The semisphencal shape of the coupling portion 1144 enables the couplin~~
portion 1144 to move polyaxially against the semispherical resection 1146.
Movement "against" the semispherical resection refers to movement in which the coupling portion I 14~
remains substantially continuously in contact with the semispherical resection 1146 so as to slide against the semispherical resection 1146. Accordingly, during installation, a surgeon can position the coupling portion 1144 against the semispherical resection 1146 and then pivot the coupling portion 1144 along three perpendicular axes, without removin~~ tho coupling portion 1144 from the semispherical resection 1146. The coupling portion 1 l=1-I
simply rotates against the semispherical resection 1146.
[00170] The phrase "polyaxial motion" refers to any combination of translation andior rotation along at least two perpendicular axes. Since the coupling portion 1144 is pivotable with respect to the semispherical resection 1146 along three perpendicular axes, the couplinz~
portion 1144 is "tri-axially pivotable" with respect to the semispherical resection 1146.
[00171] When the superior facet prosthesis 1100 has been rotated to the proper orientation, the articulating surface 1122 is positioned for proper articulation against the:
coiTesponding inferior facet or inferior facet prosthesis. The orientation of the coupling portion 1144 may then be fixed with respect to the semispherical resection 1146 by ti;~htenin'.r the castle nut 1114 (or another fastener) on the fixation element 1110, thereby firmly grippin~~
the coupling portion 1144 against the semispherical resection 1146.
Accordingly. ihc coupling pohtion 1144 is "selectively polyaxially movable" with respect to the semispherical resection 1146 because the coupling portion 1144 is movable with respect to the semispherical resection 1146 along multiple perpendicular axes until the surgeon decides to fix its disposition.
[00172] In alternative embodiments (not shown) of the invention, tri-axial pivotal movement need not be provided. Rather, a coupling portion and a corresponding resection surface may have a cylindrical, flat-sided, splined, or other shape designed to enable relative translation in addition to or in place of rotation. In place of the fixation element receivin~~
aperture 1148, an elongated fixation element receiving aperture may be used to accommodate relative translation between the coupling pol-tion and a fixation element.
Alternatively, a coupling portion and a resection surface may be shaped to provide relative pivotal motion along only one or two axes.
(00173] In an alternative embodiment the implant engaging end 1154 of the castle nut 1114 (or other fastener) can be deformable such that the implant engaging end 1154 conforms under pressure to the adjacent surface of the coupling portion 1144 regardless of the angle oi~
the surface with respect to the axis of the castle nut 1114. The deformable end can be formed of a plastic such as polyethylene attached to the metal body of the castle nut 1114. but is preferably formed of a substance that hardens over time, such as a fast-curin~~ anti biocompatible resin or a material that is heated prior to insertion into the patient and hardens upon cooling to the patient's body temperature. The material that hardens over time providea more stability than the deformable material, though both provide acceptable results.
[00174] Fig. 48 also shows an angled resection 1112 and corresponding angled llat 1156 on the apposition side of the superior facet prosthesis 1100 111 COmblllatloll Wlth the semispherical resection 1148.
[00175] The surfaces of the apposition side of the coupling portion 1144 and flat 11 ~6, as well as fixation element 1110, may or may not include porous coatings to facilitate bom ingrowth to enhance the long-term fixation of the implant. Furthermore, such porous coatings may or may not include osteoinductive or osteoconductive substances to further enhance the bone remodeling into the porous coating.
[00176] Fig. 49 shows a perspective view of the vertebra 3 with a fixation element 1110 portion implant placed through the semispherical resection 1146 in the resection surface 1112 and into the bone of the pedicle 11. The fixation element 1110 is aligned and placed into the pedicle 11 in a manner similar to that of other pedicle screws for posterior stabilization vertebrae fusion procedures.
[00177] In Fig. 50, a perspective view illustrates the superior facet prosthesis 110(.1 in place around the fixation element 1110. The castle nut 1114 has not yet been installed. As shown, the coupling portion 1144 has a semispherical nut engaging surface 1152.
[00178] Fig. 51 is a top view of the superior facet prosthesis 1100, particularly showing the curved shape of the articulating surface 1122 and the semispherical Done engaging surface 1150 of the coupling portion 1144. Additionally, Fig. 51 more clearly illustrates the angled flat 1156 on the apposition side of the superior facet prosthesis 1100.
[00179] Fig. 52 is an illustration of a rear view of the superior facet prosthesis 11 ()(?.
In this context, "rear" means as viewed from along the axis of the fixation element receiving aperture 1148. Fig. 52 particularly shows the curved shape of the articulating surlnce 1 I ??
and the semispherical nut engaging surface 1152 of the coupling portion 1144.
[00180] Fig. 53A shows a kit including a plurality of differently configured superior facet prostheses 1100, 1162, 1164, 1166, 1168. View A is a rear view of the superior facet prostheses 1100, 1162, 1164, 1166, 1168, while View B illustrates a perspective view of the laterally adjacent prosthesis 1100, 1162, 1164, 1166, 1168 rotated 90°.
As shown, the superior facet prostheses 1100, 1162, 1164, 1166, 1168 have differing physical dimensions.
[00181] Referring again to Fig. 51, which shows a single superior facet prosthesis 1100, some of the physical dimensions that change between the differently sizes superior facet prostheses 1100, 1162, 1164, 1166, 1168 in the kit (Fig. 53A) are a resection an<~le lu).
an x offset (X~), a y offset (Y~), a facet angle ((3), and a facet articulation radius (R).
Exemplary values for the foregoing will be provided below. Although the exemplary values relate primarily to LS superior and L4 inferior, they may apply to other combinations o I
vertebrae in the lower back and/or the sacrum. One or more of these variables can chan;~
between the different superior facet prosthesis sizes.
[00182] P1 is the most medial and anterior point on the auiculating surface 11?''. The superior pedicle axis 1170 is the axis that is colinear with the longitudinal axis of the fixation element 1110 that is positioned through the pedicle 11 nearest to the resected superior I-acet (not shown). The superior pedicle axis 1170 extends tlwough a saddle point S
1, which is offset as shown, by an offset 1176, which may be about 2 mm, from the fixation element receiving aperture 1148. The superior pedicle axis 1170 is parallel with the direction of the y offset (Y,). The direction of the x offset (X~) is perpendicular to the direction of the y oftset (Y~). The direction of the x offset (X~) is generally, but not precisely, lateral to medial with respect to the central axis of the patient's spine.
[00183] P4 is the most posterior point on the articulating surface 1122. As shown, f4 is displaced from the saddle point S1 by an x offset (X4) and a y offset (Ya).
The direction oi~
the X4 offset is parallel to that of the Xi offset, and the direction of the Y,~ offset is parallel to that of the YI offset.
[00184] The resection angle (a) for the superior facet prostheses 1 100 can ran~~e from 5° to 85°. However, the optimal range of the resection angle (a) for the majority of patients will range from 30° to 70°. Thus, by way of example, a family containing nine sets of superior facet prostheses 1100 can be provided with the resection angles (a) varynyr in increments of 5°. Sets of superior facet prostheses 1100 would be provided with resection angles (a) at 30°, 35°. 40°, 45°, 50°, 55°, 60°, 65° and 70°.
[00185] The x offset (X~) for the superior facet prosthesis 1100 can range from 5 mm to 30 mm. However, for the majority of patients, the x offset (Xi) will range from LU mm to 20 mm. Therefore a family of superior facet prostheses 1100 can be provided with the x offset (X~) varying in increments of 5 mm. Thus, sets of superior facet prostheses 11()t) would be provided with x offset (X~) at 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, and 20 mm to provide superior facet prostheses 1100 that cover the statistical range for the majority of the population of patients needing superior facet prostheses 1100.
[00186] The y offset (YI) for the superior facet prosthesis 1100 can range fiom ? mm to 20 mm. However, for the majority of patients, the y offset (Y~) will range ti-om 5 mm to 15 mm. Therefore a family of superior facet prostheses 1100 can be provided with the v offset (Y1) varying in increments of 2 mm. Thus, sets of superior facet prostheses I I C)() would be provided with y offset (Yl) at 5 mm, 7 mm, 9 mm, 11 mm, 13 mm, and 15 mm to provide superior facet prostheses 1100 that cover the statistical range for the majority of the population of patients needing superior facet prostheses 1100.
[00187] The x offset (X4) for the superior facet prosthesis 1100 can range from about ~
mm to about 25 mm. However, for the majority of patients, X~ will range from about 8 mm to about 20 mm. A family of superior facet prostheses may be provided with X.~
values varying in increments of 2 mm. Thus, sets of superior facet prostheses 1100 would hr-provided with X4 values of 8 mm, 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, and 2U mm to provide superior facet prostheses 1100 that cover the statistical range for the majority oi° the population of patients needing superior facet prostheses 1100.

[00188] The y offset (Yø) for the superior facet prosthesis 1100 can range ir0111 about -to about 15 mm. However, for the majority of patients, Y4 will range tiom about -? mm to about 10 mm. A family of superior facet prostheses may be provided with Ya values vaiyin'~
in increments of 2 mm. Thus, sets of superior facet prostheses 1100 would be provided with Y4 values of -2 mm, 0 mm, 2 mm, 4 mm, 6 mm, 8 mm, and 10 mm to provide superior facet prostheses 1100 that cover the statistical range for the majority of the population of patients needing superior facet prostheses 1100.
[00189] The facet angle ((3) for the superior facet prosthesis 1 100 can range ti~om ~i)w to 120°. However, for the majority of patients, the facet angle ([3) will range ti~om 6U° to 100°. Therefore a family of superior facet prostheses 1100 can be provided with the facet angle ((i) varying in increments of 5°. Thus, sets of superior facet prostheses I 100 would be provided with the angle ((3) at 60°, 65°, 70°, 75°, 80°, 85°, 90°, 95°, and 100° to provide superior facet prostheses 1100 that cover the statistical range for the majority of the population of patients needing superior facet prostheses 1100.
[00190] Once the surgeon assesses the anatomy of the superior facet that is bein~~
replaced, a particular superior facet prosthesis 1100 is selected that has the curvature and overall angle of the articulating surface 1122, with respect to the flange 1116 that best fits the:
anatomy of the level of vertebra, the left or right side, and the size of the patient's anatomy being replaced. Thus a kit containing various sizes and shapes of superior facet prostheses 1100 is provided to the surgeon and the surgeon selects the superior facet prosthesis 1100 that best suits the situation.
[00191] According to one example, such a kit may contain nine prostheses, which may be dimensioned to provide a variety of combinations of values for a, X,, Yi, (3, Xa, Y~, and R, within the ranges listed above. If desired, one or more of the above-listed variables may remain constant over the entire kit. For example, R may have a constant value, such as 1 1.5 mm, for all members of the kit.
[00192] The prostheses 1100, 1162, 1164, 1166, 1168 of the lcit of Fig. 53A
are nc~t simply scaled up or down, but are varied according to a number of carefully selected parameters to cover the vast majority of morphologies occurring in the LS
vertebra. In n similar manner, a plurality of inferior facet prostheses adapted to replace inferior facets can be provided either as a separate kit, or in combination with the kit of Fig.
53A. SLICK a Icit will be shown and described in connection with Fig. 53D.
[00193] Figs. 53B and 53C illustrate top and side views, respectively, of an exemplayv inferior facet prosthesis 1172. The inferior facet prosthesis 1172 has an x offset (X), a y offset (Y), and a z offset (Z), which are illustrated in Figs. 53B and 53C. As shown, the offsets X, Y, and Z run between a saddle point Sl of the inferior facet prosthesis 1172 and a center point C1 of the articulation surface 1174. The saddle point S1 of Figures 53B and 53C
is defined in a manner similar to that of the superior facet prosthesis 1100 of Fig. 51.
[00194] As shown in Figs. 53B and 53C, the inferior facet prosthesis 1172 has a semispherical coupling portion similar to the coupling portion 1144 of the superior lacer prosthesis 1100 introduced in the description of Fig. 47. Accordingly, the inferior facet prosthesis 1172 provides the same type of tri-axial pivotal motion during installation as the coupling portion 1144, as described previously. The coupling portion of the inferior facet prosthesis 1172 may also be nested in the coupling portion 1144 of the superior facet prosthesis 1100, or vice versa, to enable independent polyaxial adjustment of the prostheses 1100, 1170 when positioned in engagement with a single semispherical resection 1146.
[00195] Referring to Fig. 53D, a perspective view illustrates a lcit of inferior facet prostheses 1180, 1182, 1184, 1186, 1188, 1190. Again, the physical dimensions can vary between the various inferior facet prostheses 1180 in the kit of Fig. 53D.
These dimensions may include an inferior resection angle (Ia), an inferior x offset (X), an inferior y offset (h'), an inferior facet angle (I[i), an inferior facet articulation radius (IR), and an inferior z offset (Z, from the center of fixation to the center of the articulation radius).
[00196] The inferior resection angle Ia is the angle of the flat resection to be made in the vertebra, for example, the vertebra 101 illustrated in some of the preceding drawings, to serve as a backing for the articulating surface of the selected inferior facet prosthesis 1180.
1182, 1184, 1186, 1188, or 1190. When measured according to the coordinate system established for the superior facet prosthesis 1100, as illustrated in Fig. 51, the inferior resection angle Ia may be approximately the same as the facet angle (3 for the superior prosthesis 1100 because the articulation surfaces 1122, 1174 are to be positioned generally parallel to each other. Due to the clearance between the articulating surfaces 1122, 1174 and the generally concave and convex shapes thereof, as long as the selected inferior Facet prosthesis 1180, 1182, 1184, 1186, 1188, or 1190 is placed so that the articulating surfaces 1122, 1174 are generally parallel to each other, proper articulation may be expected to occur.
[00197] Thus, the inferior facet prosthesis 1180, 1182, 1184, 1186, 1188, or 119() may be dimensioned such that Ia is nearly the same as (3, and the orientation of the articulatinr~
surface 1174 may be adjusted as needed to permit the inferior facet prosthesis 1180, 1 182, 1184, 1186, 1188, or 1190 to be attached to the corresponding vertebra 101.
Accordin~~ly, Ic!
need not be determined based on measurement of the vertebra 101, but play instead h~

infeiTed based on the selection of the superior facet prosthesis 1100, 1162, 1164, 1166, or 1168 and adjusted during installation.
[00198] The inferior facet angle I/3 may be defined as the angle of the surface to which the articulating surface 1174 is most nearly parallel. Due to the shape of the inferior facet prostheses 1180, 1182, 1184, 1186, 1188, or 1190, this angle is the same as the inferior resection angle Ia, when measured according to the coordinate system of the superior facet prosthesis 1100 of Fig. 51.
[00199] The inferior pedicle axis 1170 is the axis that is collinear with the longitudinal axis of the fixation element 1110 that is positioned through the pedicle 11 nearest to the resected inferior facet (not shown). This axis is parallel with the direction of the inferior v offset (Y). The direction of the inferior x offset (X) is perpendicular to the direction of the inferior y offset (Y). The direction of the inferior x offset (X) is generally lateral to medial with respect to the central axis of the patient's spine. The direction of the inferior y offset (Y) is generally anterior to posterior. The direction of the inferior z offset (Z) is generally cephalad to caudal.
[00200] The inferior x offset (X) for the inferior facet prosthesis I 180 can range from ~ >
mm to 20 mm. However, for the majority of patients, the inferior x offset (X) will range from 2 mm to 16 mm. Therefore a family of inferior facet prostheses 1180 can be prcwided with the inferior x offset (X) varying in increments of 2 mm. Thus, sets of inferior facet prostheses 1180 would be provided with inferior x offset (X) at 2 mm, 4 mm, 6 imn, 8 mm.
mm, 12 mm, 14 mm, and 16 mm to provide inferior facet prostheses 1180 that cover the statistical range for the majority of the population of patients needing inferior facet prostheses 1180.
[00201] The inferior y offset (Y) for the inferior facet prosthesis 1180 can range ii~om -mm to 5 mm. However, for the majority of patients, the inferior y offset (Y) will rang from -12 mm to 4 mm. Therefore a family of inferior facet prostheses 1180 can be provided with the inferior y offset (Y) varying in increments of 2 mm. Thus, sets of inferior facet prostheses 1180 would be provided with inferior y offset (Y) at -12 mm, -10 mm, -8 mm, -c~
mm, -4 mm, -2 mm, 0 mm, 2 mm, and 4 mm to provide inferior facet prostheses 1180 that cover the statistical range for the majority of the population of patients needing inferior facc;t prostheses 1180.
[00202] The inferior facet articulation radius (IR) for the inferior facet prosthesis I l ~() can range from 5 mm to 30 mm. However, for the majority of patients, the inferior facet articulation radius (IR) will range from 10 mm to 15 mm. A family of incremented inferior prostheses may be provided to cover the aforementioned range. Alternatively, the inferior facet articulation radius (IR) may be set at a given value, for example, 12 mm, and such a value may be used in substantially all cases.
[00203] The inferior z offset (Z) for the inferior facet prosthesis 1180 can range ii-om 20 mm to 40 mm. However, for the majority of patients, the inferior z offset (Z) will ran~~c from 25 mm to 31 mm. Therefore a family of inferior facet prostheses 1180 can be provided with the inferior z offset (Z) varying in increments of 1 mm. Thus, sets of inferior facet prostheses 1180 would be provided with inferior z offset (Z) at 25 mm, 26 mm, 27 mm.
mm, 29 mm, 30 mm, and 31 rnm to provide inferior facet prostheses 1180 that cover the statistical range for the majority of the population of patients needing inferior facet prostheses 1180.
[00204] If desired, a lcit having ten inferior facet prostheses may be assembled. Lilce the prostheses 1100, 1162, 1164, 1166, 1168 of the kit of Fig. 53A, the prostheses 118U.
1182, 1184, 1186, 1188, 1190 of Fig. 53D are not simply scaled up or down, but are varied according to a number of carefully selected parameters to cover the vast majority of morphologies occurring in the L4 vertebra and/or other vertebrae.
[00205] The parameters of the prostheses 1100, 1162, 1164, 1166, 1168 of Fig.

and/or the prostheses 1180, 1182, 1184, 1186, 1188, 1190 of Fig. 53D may include at least two dimensions that vary among the members of the lcit independently of each other.
Dimensions that vary independently of each other need not change according to any established relationship between the dimensions, but instead, one may change while the other remains the same between any two prostheses of the kit.
[00206] Fig. 53E is a perspective view illustrating how a superior facet prosthesis 11 OO
and an inferior facet prosthesis 1180 fit together. The surgeon selects an inferior facet prosthesis that, in addition to most adequately meeting the anatomy of the patient, has an articulating surface adapted for articulating with the articulating surface of the superior facet prosthesis selected.
[00207] Fig. 53F is a dorsal view of a superior facet prosthesis 1100 and an inferior facet prosthesis 1204 attached to the LS and L4 lumbar vertebrae 102, 101. In Fig. 53F. the superior facet prosthesis 1100 is attached to the left side of the LS vertebra 102 and the inferior facet prosthesis 1204 is attached to the left L4 veuebra 101. The two prostheses 1100, 1204 are positioned on respective bone resections and oriented such that they articulate together through the range of motion naturally exhibited between the L4 and LS
vertebrae 1100, 1204. This range of motion includes flexion-extension, lateral left and right bendin~~.
torsion along a sagittal axis and combinations and coupling of all these ranges of Illot1011.
[00208] Fig. 53F shows the prostheses 1100, 1204 and vertebrae 101, 102 in a natlwal position. The articulation surface 1174 of the inferior prosthesis 1204 and the articulation surface 1122 of the superior prosthesis 1100 are in contact in the neutral position. However.
the prostheses 1100, 1204 are shaped to allow anatomic contact and articulation between the inferior facet articulation surface 1174 and the superior facet articulation surface 1122 throughout various anatomic ranges of motion.
[00209] Also shown in Fig. 53F are two planes labeled "Plane 1" and "Plane ?"
that that intersect along an axis (not shown) that passes through the contact areas of the superior facet articulation surface 1122 and the inferior facet articulation surface 1174. Plane 1 is parallel to the page of Fig. 53F, and Plane 2 is perpendicular to the page.
[00210] Fig. 53G is a posteriolaterial view of the same inferior and superior facet prostheses 1100, 1204 with the planes shown in Fig. 53F. In Fig. 53G, Plane 2 is oriented parallel to the page and plane 1 is oriented perpendicular to the page. Fig.
53G illustrates the saddle point (Sl) of the vertebra 102 to which the superior facet prosthesis 1100 is coupled, and the saddle point (S2) of the vertebra 101 to which the inferior facet prosthesis 1204 is coupled. The saddle points S1, S2 are displaced from each other along an x offset (I~) parallel to the axis at which Plane 1 and Plane 2 intersect, a y offset (IY) extendin~~
perpendicular to Plane 2, or out of the page with respect to Fig. 53G, and a z offset (1Z) extending perpendicular to Plane 1. The offsets IX, IY, and IZ may be used for implant sizing and/or selection, as will be discussed subsequently.
[00211] Fig. 53H is a posteriolateral view showing a cross-section along Plane 2. Thin cross-section view cuts through the articulation surfaces 1122, 1174 of the prostheses 1 I UU.
1204, thereby showing the convex shape of the inferior articulation surface 1174 against the concave shape of the superior articulation surface 1122.
[00212] Fig. 53H also illustrates the cephalad and caudal ends 1250, 125'' of the articulation surface 1122 of the superior facet prosthesis 1100. The articulation surface I l''?
has a radius of curvature 1254 generally about an axis 1256. However, since the radius uC
curvature 1254 changes along the articulating surface 1122, the axis 1256 may be the center of curvature for only a portion of the articulation surface 1122. The radius of culvattn-e 1254 is shown extending fiom the axis 1256 to the articulation surface 1122 in Fig.
531-1.
Furthermore, Fig. 53H illustrates a longitudinal axis 1258 of the spine in general. The axis 1256 is angled from the axis 1258 by an offset angle 1259. Since the axis 1256 and the axis 1258 may not both be precisely parallel to Plane 2, the offset angle 1259 may have a component that extends out of the page with respect to the view of Fig. 53H.
[00213] Fig. 53I is a cephalad view showing a cross-section along Plane 1.
This cross-section cuts through the articulation surfaces 1122, 1174 of the prostheses showin~~ the convex shape of the inferior articulation surface 1174 against the concave shape of the superior articulation surface 1122. Each of the articulating surfaces 1122, 1174 has a curved shape. The articulating surfaces 1122, 1174 of the superior and inferior prostheses 11Ue1_ 1204, respectively, are shaped and relatively positioned to articulate against each other such that a medial-lateral range of relative motion between the first and second vertebrae 101. I ()?
increases significantly with flexion (i.e., forward bending) of the spine.
[00214] A "significant" increase in the medial-lateral range of motion refers to a difference in the range of motion that approximates the natural motion of the spine to a degree sufficient to be noticeable by the patient. More precisely, a "significant" increase may refer to the existence of at least one additional millimeter of clearance between articulatin~~
surfaces of a facet joint under flexion, as compared to the same facet joint under extension.
Furthermore, a "significant" increase in the medial-lateral range of motion may refer to the existence of two additional millimeters of clearance between the articulating surfaces.
[00215] As shown in Fig. 53H, one of the articulating surfaces 1122, 1174, for example, the articulating surface 1122 of the superior facet prosthesis 1100, has a cephalad end 1250 and a caudal end 1252. The articulating surface 1122 also has a radius of curvature 1254 about an axis 1256 extending generally from the cephalad end 1250 end to the caudal end 1252. The radius of curvature 1254 changes along the axis 1256 to provide '~rcater clearance between the articulating surfaces 1122, 1174 when the spine is under flexion.
Similarly, the changing radius of curvature 1254 provides less clearance between the articulating surfaces 1122, 1174 when the spine is extended.
[00216] In this embodiment, the articulating surface 1122 is shaped such that, when the°
superior facet prosthesis 1100 is coupled to the vertebra, the axis 1256 is significantly anteriorly inclined at the cephalad end 1250 to provide greater clearance between a the articulating surfaces 1122, 1174 when the spine is under flexion. In addition to or in the alternative to variation of the radius of curvature 1254 from the cephalad end 1250 to thr caudal end 1252, the radius of curvature 1254 could vary along a medial-lateral direction o the articulating surface.
[00217] More precisely, with brief reference to Fig. 51 again, the radius of curvature may be larger toward a medial end 1260 and a lateral end 1262 of the articulating suriacc 1122 than at a central portion 1264 thereof. The radius of curvature could also be substantially infinite toward the medial and lateral ends, such that the articulating surface oC
the superior prosthesis has a curved region 1268 proximate the central portion 1264, a first tangent flat 1270 disposed medially of and tangent to the curved region 1268, and a second tangent flat 1272 disposed laterally of and tangent to the curved region 1268.
[00218] If desired, the inferior facet prosthesis may have an articulating surface with n three-dimensionally curved, generally elliptical shape. A three-dimensionally curved.
generally elliptical shape may have the appearance of a stretched spheroid or the like:.
Accordingly, a three-dimensionally curved, generally elliptical shape has a first cross section having a generally elliptical shape and a second cross section perpendicular to the first cross section, having a semicircular shape. Alternatively, an inferior facet prosthesis may have an articulating surface with a generally cylindrical or semispherical shape, as illustrated in connection with Figs. 40, 53B, and 53C, for example.
[00219] According to one alternative embodiment, the articulating surface of the superior facet prosthesis may have a uniform, substantially unchanging radius of curvature:.
The relative medial-lateral motion between the vertebra and the adjacent vertebra may still increase significantly with flexion of the spine due to the curvature of the inferior i-hcct prosthesis. The radius of curvature of the articulating suuace of the inferior facet prosthesis may change along an axis thereof, either along the cephalad-caudal direction or along the medial-lateral direction, to provide greater clearance between the articulating surfaces when the spine is under flexion. According to yet another alternative, the variation in motion in the medial-lateral direction may be obtained, not through a variable radius of cmvattwe. but rather, through the relative positioning of the superior and inferior facet prostheses.
[00220] Returning to Figs. 53F, 53G, 53H, and 53I, the materials used to construct the articulating surfaces of the prostheses 1100, 1174 may be selected from a group consisting ol' a polymeric material, a polymeric bearing material attached to a metal substrate, a ceramic bearing material, a metal bearing material, and combinations thereof. A
variety of surtnce coatings, treatments, and the like may be used to enhance the performance and/or longevity of the prostheses 1100, 1174.
[00221] The superior facet prosthesis 1100 may be shaped such that, when the superior facet prosthesis 1100 is coupled to the vertebra 102, the axis 1256 is significantly anteriorly inclined from a longitudinal axis (not shown) of the spine to provide greater clearance between the articulating surfaces 1122, 1174 when the spine is under flexion.
In this application, "significantly anteriorly inclined" refers to the presence of a deliberate offset.

from the longitudinal axis of the spine, that has a meaningful effect on the facet joint oC
which the corresponding prosthesis is a part. The offset angle 1259 between the axis I?~G
and the longitudinal axis 1258 of the spine may range from about -2.5°
to about 14.5°. More:
precisely, the offset angle 1259 may range from about 5° to about 10°. Yet more precisely.
the offset angle 1259 may be about 7.25°.
[00222] Referring briefly again to Fig. 51 and Fig. 53G, one method of selectin~~
inferior and superior facet prosthesis will be described. The appropriate prosthesis of the lcit of superior facet prostheses may be selected by, for example, foaming a semicircular resection centered at a position along the pedicle axis 1170 of the vertebra 102, at a laiown displacement from the saddle point Sl. Certain offsets, such as X, and X~, as shown in Fi'~.
51, may be measured with between the saddle point Sl and the most medial and anterior point P 1.
[00223] Based on X~ and X2, values of the resection angle a and the facet angle (3 may be obtained. The values of a and (3 may be used to select the appropriate superior facet prosthesis of the kit by, for example, looking up the values of a and (1 on a lookup table or the like. The remaining dimensions of the selected superior facet prosthesis may thus be determined based on the combination of a and (3.
[00224] The appropriate prosthesis of the lcit of inferior facet prostheses may also be selected by making a limited number of measurements. More precisely, a semicircular resection may be formed at a position centered along the pedicle axis of the vertebra 101, at a known displacement from the saddle point S2. One or more of the offsets IX, IY, and IZ may be measured between the resections of the saddle points S 1 and S2.
[00225] Based on the values of IX, IY, and/or IZ obtained, the values of Ia and Z (as illustrated in Fig. 53C) are determined. The values of la and Z may be used to select the appropriate inferior facet prosthesis of the kit by, for example, looking up the values of Icy and Z on a lookup table or the like. The remaining dimensions of the selected inferior dcet prosthesis may thus be determined based on the combination of Ia and Z.
[00226] The above-described selection method is beneficial because a relatively small number of linear measurements may be made to determine which set of prostheses is most appropriate for a given patient. Ease of measurement is important because the 1118aS111'e111C111~
must generally be performed during surgery. Accordingly, easier, more rapid measurements enable surgery to be more rapidly and safely carried out. In alternative embodiments.
different measurement schemes may be carried out, and may include different liner measurements, angular measurements, and the like. In this application, measurin~~ the "relative positions" of bony landmarks may include measurement of linear displacements.
angular displacements, or any combination thereof.
[00227] In alternative embodiments, a kit of superior andlor inferior prosthesis need not have multiple one-piece prostheses, but may instead have multiple components designed to be assembled together to provide a prosthesis having the necessary parameters. For example, each of a plurality of semispherical bone contacting portions may be connectable to any of a plurality of articulating surfaces, via a plurality of cotmecting members. Selectin~~ o prosthesis may then entail selecting a bone contacting portion, an articulating surface. and a connecting member. The bone contacting portion, articulating surface, and connectin~.T
member may then be coupled together via set screws, adhesives, interference fits, or the like.
[0022] If desired, the manner in which the various components are attached together may also be adjustable to enable further adjustability of the dimensions of a selected prosthesis. Such a kit of components may also include additional components such as bearing surfaces, as described in connection with Fig. 16. As yet another alternative, a sin~~le prosthesis may be adjustably deformed, for example, through the use of a lever-operated manual press, a hydraulic press, or the like, to provide the desired dimensions prior to attachment to a patient's vertebra.
[00229] After a semispherical resection 1146 has been formed in a vertebra and the corresponding prosthesis has been selected, a flat resection, such as the first resection surface:
1112 of Fig. 48, may be formed. The flat resection may be contiguous with the semispherical resection 1146, or may be separated from the semispherical resection 1146 by an expanse cal' unresected bone. The determination of which prosthesis to use may also indicate to the surgeon the proper placement of the flat resection to properly receive the selected prosthesis.
After the flat resection has been formed, the selected prosthesis may be attached to the vertebra. The procedure may be the same as or similar to that described above for installation of the inferior and superior facet prostheses.
[00230] Fig. 54 is a dorsal view of a bilateral inferior facet prosthesis system 1200 in situ: The bilateral inferior facet prosthesis system 1200 is a mufti-piece uiferior and supcriar facet prosthesis that has both a right inferior facet prosthesis 1202 and a left inferior tncct prosthesis 1204 connected by a crosslink, which may take the foirn of a stabilizing bar I'_' 1 C~.
Both the right inferior facet prosthesis 1202 and the left inferior facet prosthesis 12(>4 are designed to be affixed to the top vertebra 101 at the respective inferior facet resection surfaces 121 (Fig. 19).

[00231] The bilateral inferior facet prostheses 1202, 1204 allow replacement ol' both the left and the right inferior facets. In this embodiment, the inferior prostheses are placed over left and right fixation elements 1232, 1234 that extend into the top vertebra 101. In the embodiment shown in Fig. 54, the right inferior side is articulating against a right superior facet prosthesis 1100 attached to the first resection surface 1112 (Fig. 49) of the bottom vertebra 102. Also in this embodiment, the left inferior facet prosthesis 1204 is articulating against the left natural superior facet of the bottom vertebra 102.
[00232] The stabilizing bar 1210 of the bilateral inferior prosthesis system 1200 is designed to stabilize the left inferior facet prosthesis 1204 and the right inferior i~acet prosthesis 1202 so that they are secure. The stabilizing bar 1210 also allows the left and right inferior facet prostheses 1204, 1202 to support each other rather than requiring stabilizing members to be coupled to the spine lamina or the resected inferior facet tissue. Further, the stabilizing bar 1210 can compress the left and right inferior facet prostheses 1202, 12U~1 against the resected bone to improve bony ingrowth and apposition.
[00233] As also shown in Fig. 54, the stabilizing bar 1210 is coupled to the left and right inferior prostheses 1202, 1204 by a grippiizg mechanism. The gripping mechanism may include any of a variety of structures, including clips, clamps, adhesive-bonds, threaded fasteners, and the like. In the embodiment of Fig. 54, the gripping mechanism includes fore and aft flanges 1212, 1214 that engage the stabilizing bar 1210 to fomn a groove-and-rod joint. The fore and aft flanges 1212, 1214 are compressed together with tlueaded turnbuckles 1216, 1218 to pinch the stabilizing bar 1210 there between.
[00234] The pinching action of the flanges 1212, 1214 allows the distance between the left and right inferior prostheses 1202, 1204 to be adjusted to best suit the anatomy of the patient. During surgery, the surgeon would use a tool (not shown) to compress the left and right inferior prostheses 1202, 1204 to the desired positions and then tighten the tumbuclcles 1216, 1218 to secure the stabilizing bar 1210.
[00235] Fig. 55 is a perspective view of the bilateral inferior facet prosthesis system 1200. The right inferior facet prosthesis 1202 includes a convex articulating surface 1220 that engages an articulating surface 1122 of the superior facet prosthesis 1100.
Ill one embodiment, the articulating surface 1122 of the superior facet prosthesis 1100 has a coneavc shape (Figs. 47, 51).
[00236] In this application, the term "convex" relates to a surface that bulges outward with a three-dimensional curvature. Accordingly, a convex surface is not just a sectorial portion of a cylinder, but rather, has some outward curvature along two perpendicular directions. A convex surface may be "semispherical," or in other words, may include some sectorial portion of a sphere, which may be less than a hemisphere. However, a convex surface need not be semispherical, but may instead have contouring that provides a portion of an oval, elliptical, parabolic, and/or irregular cross sectional shape. A
convex surface also need not be curved in whole or in part, but may instead have one or more planar p01't1017s.
[00237] In this application, "concave" refers to a surface with a central portion that is recessed with respect to at least two peripheral portions positioned on either side of the central portion. A concave surface may be formed by planar regions, curves, or combinations thereof. The central portion may be recessed along only one dimension, as with a surface defined by an interior section of a cylindrical wall. Alternatively, the central portion may be recessed along two perpendicular dimensions, so that the central portion is recessed with respect to at least four peripheral portions arranged around the central portion. Accordingly, the surface may include a semispherical section, a three-dimensional parabolic or ellipsoidal section, or any other three-dimensionally curved shape.
[00238] As another alternative, the central portion of a concave surface may he recessed along one direction and distended with respect to a perpendicular direction, so that the concave surface takes on a shape similar to that of the rounded groove of a pulley that is designed to receive a rope. Like a convex surface, a concave surface need not be curved in whole or in part, but may instead have one or more planar portions.
[00239] Fig. 56 is a lateral view of the bilateral inferior facet prosthesis system 1?0() and superior facet prosthesis 1100. The right inferior prosthesis 1202 includes a member 1230 upon which the flanges 1212, 1214 clamp. In the embodiment shown, the member 1230 is a ball-shaped member 1230 upon which the flanges 1212, 1214 clamp to form a ball-and-socket joint. The ball-and-socket joint and groove-and-rod joint provide multiple degrees of freedom for variable positioning of the left and right inferior prostheses 1202, 1204. More precisely, the ball-and socket joint enables tri-axial rotation, i.e., rotation about tlwee perpendicular axes, until the flanges 1212, 1214 are pressed about the member 1230 to resist further relative rotation.
[00240] The ball-and-socket joint enables relative motion between the inferior prostheses 1202, 1204 along the anterior/posterior directions and along the cephaladJcaudal directions. The groove-and-rod joint enables relative motion between the inferior prostheses 1202, 1204 along the lateral/medial directions. However, when the turnbuckles 1 ? 16. 1 '? 1 are tightened, the displacement between the ball-shaped members 1230 of the inferior prostheses 1202, 1204 becomes fixed, and the ball-shaped members 1230 are no loner ii~eely pivotable with respect to the flanges 1212, 1214. Thus, the relative positions and orientations of the inferior prostheses 1202, 1204 may be fixed by tightening the turnbuckles 1216, 12 I ~.
[00241] An alternative embodiment replaces the ball shaped member 1230 with a member (not shown) of differing shape and flanges adapted to engage the alternatme member. Other potential shapes that allow a range of adjustability and movement between the left and right inferior prostheses 1202, 1204 and the flanges 1212, 1214 prior to clampin~~
include, but are not limited to, columnar and annular shapes.
[00242] The ball-shaped member 1230 shown in Fig. 56 has several divots founed thereon. Upon compression of the flanges 1212, 1214, the flanges deform into the divots to provide enhanced coupling and resistance to slippage therebetween. An alternative embodiment of the ball-shaped member 1230 has circumferential or axial spliiles (Fi~~. (a3 ) formed thereon, which "bite" into the flanges 1212, 1214. Other alternative surface feat<ires of the ball-shaped member 1230 include knurling, nubs, grooves, facets, and combinations ol' any of the above.
[00243] Similarly, the stabilizing bar 1210 can have surface features to enhance coupling to the flanges 1212, 1214. Exemplary surface features include longitudinal splines.
knurling, divots, nubs, and grooves. Splines prevent rotation of the stabilizing bar 121 il with respect to the flanges 1212, 1214. Knurling advantageously prevents both rotation and translation of the stabilizing bar 1210 with respect to the flanges 1212, 1214.
[00244] The flanges 1212, 1214 can be foamed of a material softer than that of the stabilizing bar 1210 and the ball-shaped members 1230 to further enhance coupling.
Illustrative materials for the stabilizing bar 1210 and ball-shaped members 1230 are Cobalt-Chrome (Co-Cr) alloys, Titanium (Ti) and stainless steel alloys. However, other biocompatible materials such as rigid polymers including PEEK and PEAK can be loaned into the shapes of the stabilization bar 1210, and/or the ball-shaped members 1230. In one alternative embodiment, the flanges 1212, 1214 are formed integrally with or rigidly attached to the left and right inferior prostheses 1202, 1204.
[00245] Referring again to Fig. 54, ends of the flanges 1212, 1214 that engage the stabilizing bar 1210 are angled towards each other. This angling avoids interference with surrounding bone and avoids interference with the superior facet or the superior fact prosthesis 1100.
[00246] With continued reference to Fig. 54, it is seen that the heads of the turnbucl<lea 1216, 1218 can vary in size. As shown, the turnbuclde 1216 is larger than the tumbuclcle 1218. The larger head of the turnbuckle 1216 allows the surgeon to exert more torque on the turnbuclele 1216, thereby allowing a more secure coupling of the flanges 1212, 1211 to the stabilizing bar 1210. The smaller head of the turnbuclele 1218 requires less space at the surgical site of the patient than the larger head of the turnbuclde 1216.
Therefore, the surgeon can select a turnbuckle head having the desired size, weighing the benefits of more applied torque of the larger head with the reduced spatial requirements of the smaller head.
[00247] An alternative embodiment replaces the stabilizing bar 1210 with a filexible link, such as a cable of a biocompatible material. Yet another alternative embodiment includes a stabilizing bar having threaded ends. Instead of pinching flanges, the threaded ends of the stabilizing bar extend through flanges of the left and right inferior prostheses 1202, 1204. Threaded fasteners engage the threaded ends of the stabilizing bar. 'fh~
threaded fasteners are then tightened to provide the desired positioning of the left and ri~~ht inferior prostheses 1202, 1204. In another variation, the stabilizing bar is rotated such that the threads of the stabilizing bar engage fixed threaded portions of the flanges.
[00248] Fig. 57 is a cranial view of the bilateral inferior facet prosthesis system 1?00.
[00249] Fig. 58 is a bottom in situ view of the bilateral inferior facet prosthesis system 1200 in situ.
[00250] Fig. 59 is rear view of the bilateral inferior facet prosthesis system 1?00 in isolation.
[00251] Fig. 60 is a top view of the bilateral inferior facet prosthesis system 1200.
[00252] Fig. 61 is a bottom view of the bilateral inferior facet prosthesis system 1200.
[00253] Fig. 62 is a perspective view of the right inferior prosthesis I 204.
[00254] Fig. 63 and 64 are perspective and end views, respectively, of various ball-shaped members 1240, 1242, 1244 that may be included in the inferior prostheses 1202. 1204 in place of the members 1230, the ball-shaped members 1240, 1242, 1244 having differin~~
surface features, particularly circumferential grooves 1302, longitudinal grooves 1304, and knurling 1306.
[00255] Fig. 65 is a dorsal view of the bilateral inferior facet prosthesis system 1200.
in which castle nuts 1320 are attached to the left and right fixation elements 1232, 1234 and to the fixation member 1110.
[00256] While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not by way ol' limitation. Thus, the breadth and scope of the invention should not be limited by any oi° the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents.

Claims

1. An implant for replacing at least a portion of a facet of a mammalian vertebra, the implant comprising:
a fixation element implantable into the vertebra;
a coupling portion shaped to be coupled to the fixation element, the coupling portion having a bone engaging surface shaped to engage a resection in the bone of the vertebra in such a way as to selectively allow polyaxial rotation of the coupling portion against the vertebra; and an articulating surface attached to the coupling portion, wherein the articulating.:
surface is shaped and positioned to articulate against a second facet surface.

2. The implant of claim 1, wherein the fixation element comprises a porous coating that facilitates bone ingrowth.

3. The implant of claim 2, wherein the porous coating comprises a substance selected from the group consisting of osteoconductive, osteoinductive and osteogenic substances.

4. The implant of claim 1, wherein the bone engaging surface of the coupling portion comprises a porous coating that facilitates bone ingrowth.

5. The implant of claim 4, wherein the porous coating comprises a substance selected from the group consisting of osteoconductive, osteoinductive and osteogenic substances.

6. The implant of claim 1, wherein the bone engaging surface is shaped to engage the resection in such a way as to selectively allow triaxial rotation of the coupling portion against to the vertebra.

7. The implant of claim 6, wherein the bone engaging surface of the coupling portion protrudes into the vertebra to engage an inversely-shaped portion of the resection.

8. The implant of claim 7, wherein the bone engaging surface of the coupling portion has a generally semispherical shape and the inversely-shaped portion of the resection comprises a generally semispherical shape.

9. The implant of claim 6, wherein the coupling portion is coupled to the fixation element in such a way as to selectively allow polyaxial movement of the coupling portion with respect to the fixation element.

10. The implant of claim 9, wherein the fixation element extends through an aperture of the coupling portion, the aperture having a diameter larger than an outer diameter of the fixation element adjacent to the aperture, wherein the outer diameter is taken in a direction perpendicular to a longitudinal axis of the fixation element.

11. The implant of claim 9, further comprising a fastener for coupling the couplings portion to the fixation element, the fastener having an implant engaging end engaging the coupling portion, the implant engaging end having a shape generally conforming to a surface of the coupling portion proximate thereto.

12. The implant of claim 9, further comprising a fastener for coupling the coupling portion to the fixation element, the fastener having an implant engaging end engaging the coupling portion, wherein the implant engaging end is deformable under pressure to conform to a surface of the coupling portion proximate thereto.

13. The implant of claim 1, wherein the articulating surface is constructed of a material selected from the group consisting of a polymeric bearing material attached to a metal substrate, a ceramic bearing material, a metal bearing material, and combinations thereof.

14. The implant of claim 1, wherein the articulating surface comprises a convex shape.

15. The implant of claim 13, wherein the articulating surface comprises a proximal end positioned relatively nearer the vertebra, a distal end positioned relatively further from the vertebra, wherein the articulating surface curves such that the proximal and distal ends both extend away from the coupling portion.

16. The implant of claim 1, wherein a component selected from the group consisting of the fixation element and a nut coupled to the fixation element is actuatable to fix a position and orientation of the bone contacting surface with respect to the resection.

17. The implant of claim 1, wherein the coupling portion is separate from the fixation element and is shaped to be gripped against the vertebra by the fixation element.

18. An implant for replacing at least a portion of a facet of a mammalian vertebra the implant comprising:
a coupling portion shaped to be coupled to a fixation element implantable into the vertebra, the coupling portion having a bone engaging surface with a semispherical shape that protrudes into the vertebra to engage a semispherical resection of the vertebra in such a way as to selectively allow polyaxial pivotal movement of the coupling portion against the vertebra; and an articulating surface attached to the coupling portion, wherein the articulating surface is shaped and positioned to articulate against a second facet surface.

19. The implant of claim 18, wherein the coupling portion is coupled to the fixation element in such a way as to selectively allow polyaxial movement of the coupling portion with respect to the fixation element.

20. The implant of claim 19, coupling portion comprises an aperture through which the fixation element extends, the aperture having a diameter larger than an outer diameter of the fixation element adjacent to the aperture, wherein the outer diameter is taken in a direction perpendicular to a longitudinal axis of the fixation element.

21. A method for replacing a facet of a mammalian vertebra, the method comprising the steps of:
resetting at least a portion of the facet;
positioning a prosthetic facet against the vertebra;
polyaxially rotating the prosthetic facet against the vertebra such that the prosthetic facet is positioned to articulate against a second facet; and fixedly attaching the prosthetic facet to the vertebra.

22. The method of claim 21, wherein polyaxially rotating the prosthetic facet comprises triaxially rotating the prosthetic facet.

23. The method of claim 22, wherein the prosthetic facet comprises a bone engaging surface, wherein attaching the prosthetic facet to the vertebra comprises positioning the bone engaging surface to protrude into the vertebra to engage an inversely-shaped portion of a resection formed by resetting at least a portion of the facet.

24. The method of claim 23, wherein the bone engaging surface has a generally semispherical shape and the inversely-shaped portion of the resection comprises a generally semispherical shape.

25. The method of claim 21, further comprising actuating a component selected from the group consisting of the fixation element and a nut coupled to the fixation element to fix a position and orientation of the bone engaging surface with respect to the resection.

26. A method for establishing a disposition of an implant for replacing a facet of a mammalian vertebra, the implant comprising an articulating surface and a coupling portion, the coupling portion having a bone engaging surface, wherein the articulating surface is shaped to articulate against a second facet surface, the method comprising:
forming a semispherical resection in the vertebra;
positioning the bone engaging surface against the semispherical resection such that the articulating surface is positioned to articulate against a second facet;
and affixing the of the bone engaging surface against the semispherical resection.

27. The method of claim 26, wherein the implant further comprises a fixation element, the method further comprising implanting the fixation element into the vertebra, wherein affixing the bone engaging surface against the semispherical resection comprises tightening a component selected from the group consisting of the fixation element and a nut coupled to the fixation element.

28. The method of claim 26, wherein forming the rounded resection comprises forming a rounded concave resection.

29. A method for establishing a disposition of an implant for replacing a facet of a mammalian vertebra, the implant comprising an articulating surface and a coupling portion.
the coupling portion having a bone engaging surface, wherein the articulating surface is shaped to articulate against a second facet surface, the method comprising:
forming a rounded resection in the vertebra;
forming a substantially flat resection in the vertebra, proximate the rounded resection:
positioning the bone engaging surface against the rounded resection such that the articulating surface is positioned to articulate against the second facet surface; and affixing the bone engaging surface against the rounded resection.

30. The method of claim 29, wherein the implant further comprises a fixation element, the method further comprising implanting the fixation element into the vertebra, wherein affixing the bone engaging surface against the rounded resection comprises tightening a component selected from the group consisting of the fixation element and a nut coupled to the fixation element.

31. The method of claim 29, wherein forming the rounded resection comprises forming a rounded concave resection.

32. The method of claim 29, wherein forming the rounded resection comprises forming a semispherical resection.

33. The method of claim 29, wherein forming the substantially flat resection comprises positioning the substantially flat resection contiguous with the rounded resection.

34. The method of claim 33, wherein the implant comprises an angled flat, wherein positioning the bone engaging surface against the rounded resection comprises positioning the angled flat to lie against the substantially flat resection.

35. The method of claim 29, further comprising measuring relative dispositions of a plurality of bony landmarks of the vertebra to obtain morphology data.

36. The method of claim 35, wherein the relative dispositions of the bony landmarks are measured after formation of the rounded resection, and before formation of the substantially flat resection.

37. The method of claim 36, wherein forming the substantially flat resection in the vertebra comprises utilizing the morphology data to determine a desired disposition of the substantially flat resection.

38. A facet prosthesis system for replacing an inferior facet of a first vertebra of a spine, and a superior facet of a second vertebra of the spine, the system comprising:
an inferior prosthesis shaped to be coupled to the first vertebra, the inferior prosthesis having an inferior articulating surface; and a superior prosthesis shaped to be coupled to the second vertebra, the superior prosthesis having a superior articulating surface;
wherein the articulating surfaces of the inferior and superior prostheses are shaped and relatively positioned to articulate against each other such that a medial-lateral range of relative motion between the first and second vertebrae decreases significantly with extension of the spine.

39. The system of claim 38, wherein each of the articulating surfaces has a curved shape, wherein one of the articulating surfaces has a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature changes along the axis to provide greater clearance between the articulating surfaces when the spine is flexed.

40. The system of claim 39, wherein the articulating surface of the superior prosthesis has a concave shape having the cephalad end, caudal end, and radius of curvature, wherein the radius of curvature increases toward the cephalad end.

41. The system of claim 38, wherein each of the articulating surfaces has a curved shape.
wherein one of the articulating surfaces has a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the prosthesis is shaped such that, when the prosthesis is coupled to the vertebra, the axis is significantly anteriorly inclined to provide greater clearance between the articulating surfaces when the spine is flexed.

42. The system of claim 41, wherein the articulating surface of the superior prosthesis has a concave shape having the cephalad, caudal end, and radius of curvature, wherein the axis is anteriorly inclined toward the cephalad end.

43. The system of claim 42, wherein the axis is inclined at an angle of at least five degrees with respect to a longitudinal axis of the spine.

44. The system of claim 38, wherein each of the articulating surfaces has a curved shape.
wherein one of the articulating surfaces has a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature varies along a medial-lateral direction of the articulating surface.

45. The system of claim 44, wherein the articulating surface of the superior prosthesis has a concave shape having the cephalad end, caudal end, and radius of curvature, wherein the articulating surface of the superior prosthesis has a medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the medial and lateral ends than at the central portion.

46. The system of claim 45, wherein the radius of curvature is substantially infinite toward the medial and lateral ends, such that the articulating surface of the superior prosthesis has a curved region proximate the central portion, a first tangent flat disposed medially of and tangent to the curved region, and a second tangent flat disposed laterally of and tangent to the curved region.

47. The system of claim 44, wherein the articulating surface of the superior prosthesis has a concave shape and the articulating surface of the inferior prosthesis has a convex shape.

48. The system of claim 47, wherein the articulating surface of the inferior prosthesis has a three-dimensionally curved elliptical shape.

49. The system of claim 38, wherein at least one of the articulating surfaces is constructed of a material selected from a group consisting of a polymeric material, a polymeric bearings material attached to a metal substrate, a ceramic bearing material, a metal bearing material, and combinations thereof.

50. A prosthesis for replacing at least a portion of a facet of a vertebra of a spine, the prosthesis comprising:
a fixation element implantable into the vertebra;
a coupling portion shaped to be coupled to the fixation element, the coupling portion having a bone engaging surface positioned to abut the vertebra; and an articulating surface attached to the coupling portion;
wherein the articulating surface is positioned and shaped to articulate against an articulating surface of an adjacent vertebra such that a medial-lateral range of relative motion between the vertebra and the adjacent vertebra decreases significantly with extension of the spine.

51. The prosthesis of claim 50, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature changes along the axis to provide greater clearance between the articulating surfaces when the spine is flexed.

52. The prosthesis of claim 51, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein the radius of curvature increases toward the cephalad end.

53. The prosthesis of claim 50, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the prosthesis is shaped such that, when the prosthesis is coupled to the vertebra, the axis is significantly anteriorly inclined to provide greater clearance between the articulating surfaces when the spine is flexed.

54. The prosthesis of claim 53, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein the axis is anteriorly inclined toward the cephalad end.

55. The prosthesis of claim 54, wherein the prosthesis is shaped such that, when the prosthesis is coupled to the vertebra, the axis is inclined at an angle of at least five degrees with respect to a longitudinal axis of the spine.

56. The prosthesis of claim 50, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature varies along a medial-lateral direction of the articulating surface.

57. The prosthesis of claim 56, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein the articulating surface of the prosthesis has a medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the medial and lateral ends than at the central portion.

58. The prosthesis of claim 57, wherein the radius of curvature is substantially infinite toward the medial and lateral ends, such that the articulating surface of the prosthesis has a curved region proximate the central portion, a first tangent flat disposed medially of and tangent to the curved region, and a second tangent flat disposed laterally of and tangent to the curved region.

59. The prosthesis of claim 50, wherein the articulating surface of the prosthesis is constructed of a material selected from a group consisting of a polymeric bearing material attached to a metal substrate, a ceramic bearing material, a metal bearing material, and combinations thereof.

60. A prosthesis for replacing at least a portion of a facet of a vertebra of a spine. the prosthesis comprising:
a fixation element implantable into the vertebra;
a coupling portion shaped to be coupled to the fixation element, the coupling portion having a bone engaging surface positioned to abut the vertebra; and an articulating surface attached to the coupling portion to articulate against an articulating surface of an adjacent vertebra, the articulating surface of the prosthesis having a cephalad end and a caudal end, wherein the articulating surface has a radius of curvature about an axis extending generally from the cephalad end to the caudal end;
wherein the axis is significantly anteriorly inclined toward the cephalad end.

61. The prosthesis of claim 60, wherein the prosthesis comprises a superior prosthesis, wherein the articulating surface of the prosthesis has a concave shape.

62. The prosthesis of claim 61, wherein the prosthesis is shaped such that, when the prosthesis is coupled to the vertebra, the axis is inclined at an angle of at least five degrees with respect to a longitudinal axis of the spine.

63. The prosthesis of claim 60, wherein the articulating surface of the prosthesis has o medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the medial and lateral ends than at the central portion.

64. A superior prosthesis for replacing at least a portion of a superior facet of a vertebra of a spine, the prosthesis comprising:
a fixation element implantable into the vertebra;
a coupling portion shaped to be coupled to the fixation element, the coupling portion having a bone engaging surface positioned to abut the vertebra; and an articulating surface attached to the coupling portion to articulate against an articulating surface of an adjacent vertebra, the articulating surface of the prosthesis having a concave shape with a variable radius of curvature, wherein the articulating surface is positioned to articulate against an inferior facet of an adjacent vertebra.

65. The superior prosthesis of claim 64, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature varies along a medial-lateral direction of the articulating surface.

66. The prosthesis of claim 65, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein the articulating surface of the prosthesis has a medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the;
medial and lateral ends than at the central portion.

67. The prosthesis of claim 66, wherein the radius of curvature is substantially infinite toward the medial and lateral ends, such that the articulating surface of the prosthesis has a curved region proximate the central portion, a first tangent flat disposed medially of and tangent to the curved region, and a second tangent flat disposed laterally of and tangent to the curved region.

68. The prosthesis of claim 64, wherein the articulating surface of the adjacent vertebra has a convex shape and the articulating surface of the prosthesis has a concave shape selected to articulate against the articulating surface of the adjacent vertebra in a manner that approximates articulation of a natural facet joint.

69. A method for replacing at least one facet of a first vertebra of a spine, the method comprising:
resecting the first vertebra to provide a resected portion of the first vertebra; and attaching a coupling portion of a prosthesis to the first resected portion to position an articulating surface of the prosthesis to articulate against an articulating surface of a second vertebra;
wherein positioning the articulating surface of the prosthesis comprises providing a medial-lateral range of relative motion between the first and second vertebrae that decreases significantly with extension of the spine.

70. The method of claim 69, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature changes along the axis, wherein providing the medial-lateral range of relative motion between the first and second vertebrae comprises providing greater clearance between the articulating surfaces when the spine is flexed.

71. The method of claim 70, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein the radius of curvature increases toward the cephalad end, wherein resecting the first vertebra comprises removing at least a portion of a natural superior facet.

72. The method of claim 69, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein positioning the articulating surface of the prosthesis comprises significantly anteriorly inclining the axis to provide greater clearance between the articulating surfaces when the spine is flexed.

73. The method of claim 72, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein resecting the first vertebra comprises removing at least a portion of a natural superior facet, wherein significantly anteriorly inclining the axis comprises inclining the axis toward the cephalad end.

74. The method of claim 75, wherein significantly anteriorly inclining the axis comprises inclining the axis at an angle of at least five degrees with respect to a longitudinal axis of the spine.

75. The prosthesis of claim 69, wherein the articulating surface of the prosthesis has a curved shape with a cephalad end and a caudal end, and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein the radius of curvature varies along a medial-lateral direction of the articulating surface, wherein providing the medial-lateral range of relative motion between the first and second vertebrae comprises providing greater clearance between the articulating surfaces when the spine is flexed.

76. The prosthesis of claim 75, wherein the prosthesis comprises a superior prosthesis, wherein the articulating surface of the prosthesis has a concave shape, wherein the articulating surface of the prosthesis has a medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the medial and lateral ends than at the central portion, wherein resecting the first vertebra comprises removing at least a portion of a natural superior facet.

77. The prosthesis of claim 76, wherein the radius of curvature is substantially infinite toward the medial and lateral ends, such that the articulating surface of the prosthesis has a curved region proximate the central portion, a first tangent flat disposed medially of and tangent to the curved region, and a second tangent flat disposed laterally of and tangent to the curved region.

78. A method for replacing at least one facet of a first vertebra of a spine, the method comprising:

resetting the first vertebra to provide a resected portion of the first vertebra; and attaching a coupling portion of a prosthesis to the resected portion to position an articulating surface of the prosthesis to articulate against a second articulating surface of a second vertebra;
wherein the articulating surface of the vertebra comprises a cephalad end and a caudal end and a radius of curvature about an axis extending generally from the cephalad end to the caudal end, wherein positioning the articulating surface of the prosthesis comprises significantly inclining the axis anteriorly toward the cephalad end.

79. The method of claim 78, wherein the prosthesis comprises a superior prosthesis.
wherein the articulating surface of the prosthesis has a concave shape, wherein resetting the first vertebra comprises removing at least a portion of a natural superior facet.

80. The method of claim 79, wherein significantly anteriorly inclining the axis comprises inclining the axis at an angle of at least five degrees with respect to a longitudinal axis of the spine.

81. The method of claim 78, wherein the articulating surface of the prosthesis has a medial end, a lateral end, and a central portion between the medial and lateral ends, wherein the radius of curvature is larger toward the medial and lateral ends than at the central portion.

82. A bilateral facet prosthesis system for replacing facets of a mammalian vertebra, the system comprising:
a first prosthesis having a first bone engaging surface shaped to seat directly against the vertebra, the first prosthesis having a first articulating surface for articulating against a first facet of an adjacent vertebra;
a second prosthesis having a second bone engaging surface shaped to seat directly against the vertebra, the second prosthesis having a second articulating surface for articulating against a second facet of the adjacent vertebra; and a crosslink adjustably attachable to extend between the first and second prostheses to fix a displacement between the first and second prostheses at any of a plurality of displacement values.

83. The system of claim 82, wherein the crosslink comprises a rod having a substantially rigid construction.

84. The system of claim 83, further comprising a first coupling coupled to the first prosthesis, the first coupling having a first gripping mechanism configured to grip the crosslink to couple the first prosthesis to the crosslink at any of a plurality of positions along an axis of the crosslink.

85. The system of claim 84, further comprising a second coupling coupled to the second prosthesis, the second coupling having a second gripping mechanism configured to grip the crosslink to couple the second prosthesis to the crosslink at any of a plurality of positions along the axis.

86. The system of claim 84, wherein the first gripping mechanism comprises flanges positionable on either side of the crosslink such that the crosslink is gripped between the flanges.

87. The system of claim 86, wherein the first gripping mechanism further comprises a first turnbuckle that is rotatable to urge the flanges together to grip the crosslink.

88. The system of claim 86, wherein the first coupling enables the first prosthesis to lockably pivot with respect to the crosslink to enable fixation of an angular displacement between the prostheses about a first axis at any of a plurality of angular displacement values.

89. The system of claim 88, wherein the flanges engage a semispherical member of the first prosthesis to provide a ball-and-socket joint.

90. The system of claim 89, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves.
circumferential grooves, facets, nubs, and combinations thereof, wherein the surface features resist relative rotation between the first coupling and the semispherical member in response to pressure urging the surface features against the flanges.

91. The system of claim 89, wherein at least one of the flanges is formed of a material that is softer than a material from which the semispherical member is formed.

92. The system of claim 86, wherein at least one of the flanges is formed of a material that is softer than a material from which the crosslink is formed.

93. The system of claim 82, wherein the first prosthesis comprises a first inferior prosthesis and the second prosthesis comprises a second inferior prosthesis, the system further comprising a first superior prosthesis having the first superior facet of the adjacent vertebra, and a second superior prosthesis having the second superior facet of the adjacent vertebra.

94. The system of claim 93, wherein an articulating surface of the first inferior prosthesis is convex and an articulating surface of the first superior facet prosthesis is concave.

95. The system of claim 82, wherein the crosslink compresses the prostheses against the vertebra.

96. A bilateral facet prosthesis system for replacing facets of a mammalian vertebra. the system comprising:

a first inferior prosthesis shaped to be coupled to the vertebra, the first inferior prosthesis having a first articulating surface for articulating against a first superior facet of an adjacent vertebra;
a second inferior prosthesis shaped to be coupled to the vertebra, the second inferior prosthesis having a second articulating surface for articulating against a second superior facet of the adjacent vertebra; and a crosslink adjustably attachable to extend between the first and second inferior prostheses to fix a displacement between the first and second prostheses at any of a plurality of displacement values.

97. ~The system of claim 96, wherein the crosslink comprises a rod having a substantially rigid construction.

98. ~The system of claim 97, further comprising a first coupling coupled to the first prosthesis, the first coupling having a first gripping mechanism configured to grip the crosslink to couple the first prosthesis to the crosslink at any of a plurality of positions along an axis of the crosslink.

99. ~The system of claim 98, further comprising a second coupling coupled to the second prosthesis, the second coupling having a second gripping mechanism configured to grip the crosslink to couple the second prosthesis to the crosslink at any of a plurality of positions along the axis.

100. ~The system of claim 98, wherein the first gripping mechanism comprises flanges positionable on either side of the crosslink such that the crosslink is gripped between the flanges.

101. ~The system of claim 100, wherein the first gripping mechanism further comprises a first turnbuckle that is rotatable to urge the flanges together to grip the crosslink.

102. ~The system of claim 100, wherein the flanges engage a semispherical member of the first inferior prosthesis to provide a ball-and-socket joint.

103. ~The system of claim 102, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves, circumferential grooves, facets, nubs, and combinations thereof, wherein the surface features resist relative rotation between the first coupling and the semispherical member in response to pressure urging the surface features against the flanges.

104. ~The system of claim 96, further comprising a first superior prosthesis having the first superior facet of the adjacent vertebra, and a second superior prosthesis having the second superior facet of the adjacent vertebra.

105. The system of claim 96, wherein the crosslink compresses the inferior prostheses against the vertebra.

106. A bilateral facet prosthesis system for replacing facets of a mammalian vertebra the system comprising:
a first prosthesis shaped to be coupled to the vertebra, the first prosthesis having a first articulating surface for articulating against a first facet of an adjacent vertebra;
a second prosthesis shaped to be coupled to the vertebra, the second prosthesis having a second articulating surface for articulating against a second facet of the adjacent vertebra:
a crosslink adjustably attachable to extend between the first and second prostheses to fix an angular displacement between the prostheses about a first axis at any of a plurality of angular displacement values.

107. The system of claim 106, wherein.the crosslink comprises a rod having a substantially rigid construction.

108. The system of claim 107, further comprising a first coupling coupled to the first prosthesis, the first coupling having a first gripping mechanism configured to grip the crosslink to couple the first prosthesis to the crosslink at any of a plurality of positions along an axis of the crosslink.

109. The system of claim 108, further comprising a second coupling coupled to the second prosthesis, the second coupling having a second gripping mechanism configured to grip the crosslink to couple the second prosthesis to the crosslink at any of a plurality of positions along the axis of the crosslink.

110. The system of claim 108, wherein the first gripping mechanism comprises flanges positionable on either side of the crosslink such that the crosslink is gripped between the flanges.

111. The system of claim 110, wherein the first gripping mechanism further comprises a first turnbuckle that is rotatable to urge the flanges together to grip the crosslink.

112. The system of claim 110, wherein the first coupling enables the first prosthesis to lockably pivot with respect to the crosslink to enable fixation of the angular displacement between the prostheses.

113. The system of claim 112, wherein the first coupling further enables fixation of an angular displacement between the prostheses about a second axis perpendicular to the first axis, at any of a plurality of angular displacement values.

114. The system of claim 112, wherein the flanges engage a semispherical member of the first prosthesis to provide a ball-and-socket joint.

115. The system of claim 114, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves, circumferential grooves, facets, nubs, and combinations thereof, wherein the surface features resist relative rotation between the first coupling and the semispherical member in response to pressure urging the surface features against the flanges.

116. The system of claim 106, wherein the first prosthesis comprises a first inferior prosthesis and the second prosthesis comprises a second inferior prosthesis, the system further comprising a first superior prosthesis having the first superior facet of the adjacent vertebra, and a second superior prosthesis having the second superior facet of the adjacent vertebra.

117. The system of claim 106, wherein the crosslink compresses the prostheses against the vertebra.

118. A bilateral facet prosthesis system for replacing facets of a mammalian vertebra, the system comprising:
a first prosthesis shaped to be coupled to the vertebra, the first prosthesis having a first articulating surface for articulating against a first facet of an adjacent vertebra;
a second prosthesis shaped to be coupled to the vertebra, the second prosthesis having a second articulating surface for articulating against a second facet of the adjacent vertebra;
a crosslink adjustably attachable to extend between the first and second inferior prostheses; and a first coupling coupled to the first prosthesis, the first coupling having a first gripping mechanism configured to grip the crosslink to couple the first prosthesis to the crosslink.

119. The system of claim 118, wherein the crosslink comprises a rod having a substantially rigid construction, wherein the first gripping mechanism is further configured to couple the first prosthesis to the crosslink at any of a plurality of positions along an axis of the crosslink.

120. The system of claim 119, further comprising a second coupling coupled to the second prosthesis, the second coupling having a second gripping mechanism configured to grip the crosslink to couple the second prosthesis to the crosslink at any of a plurality of positions along the axis.

121. The system of claim 119, wherein the first gripping mechanism comprises flanges positionable on either side of the crosslink such that the crosslink is gripped between the flanges.

122. The system of claim 121, wherein the first gripping mechanism further comprises a first turnbuckle that is rotatable to urge the flanges together to grip the crosslink.

123. The system of claim 121, wherein the first coupling enables the first prosthesis to lockably pivot with respect to the crosslink to enable fixation of an angular displacement between the prostheses about a first axis at any of a plurality of angular displacement values.

124. ~The system of claim 123, wherein the flanges engage a semispherical member of the first prosthesis to provide a ball-and-socket joint.

125. ~The system of claim 124, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves.
circumferential grooves, facets, nubs, and combinations thereof, wherein the surface features resist relative rotation between the first coupling and the semispherical member in response to pressure urging the surface features against the flanges.

126. ~The system of claim 118, wherein the first prosthesis comprises a first interior prosthesis and the second prosthesis comprises a second inferior prosthesis, the system further comprising a first superior prosthesis having the first superior facet of the adjacent vertebra, and a second superior prosthesis having the second superior facet of the adjacent vertebra.

127. ~The system of claim 118, wherein the crosslink compresses the prostheses against the vertebra.

128. ~A method for replacing facets of a mammalian vertebra, the method comprising:
resecting the vertebra to provide first and second resected portions of the vertebra:
attaching a first prosthesis to the first resected portion such that a first articulating surface of the first prosthesis is positioned to articulate against a first facet of an adjacent vertebra;
attaching a second prosthesis to the second resected portion such that a second articulating surface of the second prosthesis is positioned to articulate against a second facet of the adjacent vertebra;
selecting any one of a plurality of displacement values between the first and second prostheses; and attaching a crosslink to the prostheses after attachment of at least one of the prostheses to the vertebra such that the crosslink extends between the prostheses to provide the selected displacement value between the prostheses.

129. The method of claim 128, wherein attaching the crosslink to the prostheses comprises gripping the crosslink with a first gripping mechanism of a first coupling coupled to the first prosthesis at any of a plurality of positions along an axis of the crosslink.

130. The method of claim 129, wherein attaching the crosslink to the prostheses further comprises gripping the crosslink with a second gripping mechanism of a second coupling coupled to the second prosthesis at any of a plurality of positions along the axis.

131. The method of claim 129, wherein attaching the crosslink to the prosthesis further comprises:
positioning flanges on either side of the crosslink; and gripping the crosslink between the flanges.

132. The method of claim 131, wherein gripping the crosslink between the flanks comprises rotating a first turnbuckle to urge the flanges together.

133. The method of claim 131, further comprising fixing an angular displacement between the prostheses about a first axis at any of a plurality of angular displacement values.

134. The method of claim 133, wherein fixing the angular displacement between the prostheses comprises engaging a semispherical member of the first prosthesis with the flanges to provide a ball-and-socket joint.

135. The method of claim 134, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves, circumferential grooves, facets, nubs, and combinations thereof, wherein engaging the semispherical member comprises urging the surface features against the flanges to resist relative rotation between the first coupling and the semispherical member.

136. The method of claim 128, wherein attaching the crosslink to the prostheses comprises compressing the prostheses against the vertebra.

137. A method for replacing facets of a mammalian vertebra, the method comprising:
resecting the vertebra to provide first and second resected portions of the vertebra:
attaching a first inferior prosthesis to the first resected portion such that a first articulating surface of the first inferior prosthesis is positioned to articulate against' a first superior facet of an adjacent vertebra;
attaching a second inferior prosthesis to the second resected portion such that a second articulating surface of the second inferior prosthesis is positioned to articulate against a second superior facet of the adjacent vertebra;
selecting any one of a plurality of displacement values between the first and second inferior prostheses; and attaching a crosslink to the inferior prostheses such that the crosslink extends between the inferior prostheses to provide the selected displacement value between the inferior prostheses.

138. The method of claim 137, wherein attaching the crosslink to the inferior prostheses comprises gripping the crosslink with a first gripping mechanism of a first coupling coupled to the first inferior prosthesis at any of a plurality of positions along an axis of the crosslink.

139. The method of claim 138, wherein attaching the crosslink to the inferior prostheses further comprises gripping the crosslink with a second gripping mechanism of a second coupling coupled to the second inferior prosthesis at any of a plurality of positions along the axis.

140. The method of claim 138, wherein attaching the crosslink to the inferior prosthesis further comprises:
positioning flanges on either side of the crosslink; and gripping the crosslink between the flanges.

141. The method of claim 140, wherein gripping the crosslink between the flanges comprises rotating a first turnbuckle to urge the flanges together.

142. The method of claim 140, further comprising fixing an angular displacement between the inferior prostheses about a first axis at any of a plurality of angular displacement values.

143. The method of claim 142, wherein fixing the angular displacement between the inferior prostheses comprises engaging a semispherical member of the first inferior prosthesis with the flanges to provide a ball-and-socket joint.

144. The method of claim 143, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves, circumferential grooves, facets, nubs, and combinations thereof, wherein engaging the semispherical member comprises urging the surface features against the flanges to resist relative rotation between the first coupling and the semispherical member.

145. The method of claim 137, wherein attaching the crosslink to the inferior prostheses comprises compressing the inferior prostheses against the vertebra.

146. A method for replacing facets of a mammalian vertebra, the method comprising:
resecting the vertebra to provide first and second resected portions of the vertebra;
attaching a first prosthesis to the first resected portion such that a first articulating surface of the first prosthesis is positioned to articulate against a first facet of an adjacent vertebra;
attaching a second prosthesis to the second resected portion such that a second articulating surface of the second prosthesis is positioned to articulate against a second facet of the adjacent vertebra;

selecting any one of a plurality of angular displacement values between the first and second prostheses about a first axis; and attaching a crosslink to the prostheses such that the crosslink extends between the prostheses to fix an orientation of the first prosthesis with respect to the second prosthesis to provide the selected angular displacement value.

147. ~The method of claim 146, wherein attaching the crosslink to the prostheses comprises gripping the crosslink with a first gripping mechanism of a first coupling coupled to the first prosthesis at any of a plurality of positions along an axis of the crosslink.

148. The method of claim 147, wherein attaching the crosslink to the prostheses further comprises gripping the crosslink with a second gripping mechanism of a second coupling coupled to the second prosthesis at any of a plurality of positions along the axis.

149. The method of claim 147, wherein attaching the crosslink to the prosthesis further comprises:
positioning flanges on either side of the crosslink; and gripping the crosslink between the flanges.

150. The method of claim 149, wherein gripping the crosslink between the flanges comprises rotating a first turnbuckle to urge the flanges together.

151. The method of claim 149, further comprising fixing an angular displacement between the prostheses about a second axis perpendicular to the first axis, at any of a plurality of angular displacement values.

152. The method of claim 151, wherein fixing the angular displacement between the prostheses comprises engaging a semispherical member of the first prosthesis with the flanges to provide a ball-and-socket joint.

153. The method of claim 152, wherein the semispherical member has surface features selected from a group consisting of divots, splines, knurling, longitudinal grooves.
circumferential grooves, facets, nubs, and combinations thereof, wherein engaging the semispherical member comprises urging the surface features against the flanges to resist relative rotation between the first coupling and the semispherical member.

154. The method of claim 146, wherein attaching the crosslink to the prostheses comprises compressing the prostheses against the vertebra.

155. A spinal implant kit for replacing a removed facet of a resected vertebra, the spinal implant kit comprising:
a plurality of components;

wherein each of the components comprises a first dimension and a second dimension.
wherein the first and second dimensions vary in magnitude among the components independently of each other such that a subset of the components is selectable to provide a selected prosthesis dimensioned to match a morphology of the resected vertebra such that an articulating surface of the selected prosthesis is positioned to approximate an original position of the removed facet when the selected prosthesis is attached to the resected vertebra.

156. The spinal implant kit of claim 155, wherein the plurality of components comprises a first prosthesis and a second prosthesis, each of which is of one-piece construction and is independently selectable to provide the selected prosthesis, wherein the first dimension of the second prosthesis has a magnitude different from a magnitude of the first dimension of the first prosthesis, wherein either of the first and second prostheses is selectable to provide the selected prosthesis.

157. The spinal implant kit of claim 156, wherein the first and second prostheses comprise superior facet prostheses, wherein the removed facet is a natural superior facet.

158. The spinal implant kit of claim 157, wherein each of the first and second prostheses comprises an articulating surface, wherein the first dimension comprises a resection angle (.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the resected vertebra and the second dimension comprises a facet angle (.beta.) defining an orientation of the articulating surface.

159. The spinal implant kit of claim 158, wherein the removed facet has an articulating surface that, prior to removal of the removed facet, has a most medial and anterior point (P1), wherein the resected vertebra further has a pedicle saddle point (S1) defining an intersection between a posterior pedicle bone surface and a longitudinal axis of the pedicle, wherein the first and second dimensions are determined by measuring an x offset (X1) between S1 and P1 and a y offset (Y1) between S1 and P1 and selecting first and second dimensions that are predetermined for a given X1 value and a given Y1 value.

160. The spinal implant kit of claim 159, wherein each of the first and second prostheses further comprises an implant pedicle saddle point positioned to substantially overlie S1 when the selected prosthesis is attached to the resected vertebra and a radius of articulation (R) defining a radius of curvature of the articulating surface of the first and second prostheses.

161. The spinal implant kit of claim 157, wherein the removed facet has an articulating surface that, prior to removal of the removed facet, has a most medial and anterior point (P1).
wherein the resected vertebra further has a pedicle saddle point (S1) defining an intersection between a posterior pedicle bone surface and a longitudinal axis of the pedicle, wherein the first and second dimensions are determined by measuring an x offset (X1) between S1 and P1 and a y offset (Y1) between S1 and P1 and selecting first and second dimensions that are predetermined for a given X1 value and a given Y1 value.

162. The spinal implant kit of claim 157, wherein each of the first and second prostheses comprises an articulating surface having a most medial and anterior point (P1) and a most posterior and lateral point (P4), wherein each of the first and second prostheses further comprises a pedicle saddle point positioned to substantially overlie an implant pedicle saddle point (S1) of the resected vertebra when the selected prosthesis is attached to the resected vertebra, wherein the first and second dimensions are selected from the group consisting of a resection angle (.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the resected vertebra, an x offset (X1) between S1 and P1, a y offset (Y1) between S1 and P1, an x offset (X4) between S1 and P4, a y offset (Y4) between S1 and P4. a facet angle (.beta.) defining an orientation of the articulating surface, and a facet articulation radius (R) defining a radius of curvature of the articulating surface.

163. The spinal implant kit of claim 159, wherein .alpha. ranges in magnitude from about 30° to about 70° and .beta. ranges from about 60° to about 100°.

164. The spinal implant kit of claim 156, wherein the first and second prostheses comprise inferior facet prostheses, wherein the removed facet is a natural inferior facet.

165. The spinal implant kit of claim 164, wherein each of the first and second prostheses comprises an articulating surface having a radius of articulation (IR) defining a radius of curvature of the articulating surface and an implant pedicle saddle point positioned to substantially overlie a pedicle saddle point (S1) of the resected vertebra when the selected prosthesis is attached to the resected vertebra, wherein S1 defines an intersection between a posterior pedicle bone surface and a longitudinal axis of the pedicle, wherein the first dimension comprises a resection angle (I.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the resected vertebra and the second dimension comprises a z offset (Z) between S1 and a center of IR.

166. The spinal implant kit of claim 165, wherein the first and second dimensions are determined by measuring one or more of an x offset (IX) between S1 and a second pedicle saddle point (S2) of an adjacent vertebra, a y offset (IY) between S1 and S2, and a z offset (IZ) between S1 and S2, and selecting first and second dimensions that are predetermined for one or more of a given IX value, a given IY value, and a given IZ value.

167. The spinal implant kit of claim 164, wherein the resected vertebra further has a pedicle saddle point (S1) defining an intersection between a posterior pedicle bone surface and a longitudinal axis of the pedicle, wherein the first and second dimensions are determined by measuring one or more of an x offset (IX) between S1 and a second pedicle saddle point (S2) of an adjacent vertebra, a y offset (IY) between S1 and S2, and a z offset (Z) between S1 and S2, and selecting first and second dimensions that are predetermined for one or more of a given IX value, a given IY value, and a given IZ value.

168. The spinal implant kit of claim 164, wherein each of the first and second prostheses comprises an articulating surface having a center of a radius of articulation (IR) defining a radius of curvature of the articulating surface, wherein each of the first and second prostheses further comprises an implant pedicle saddle point positioned to substantially overlie a pedicle saddle point (S1) of the resected vertebra when the selected prosthesis is attached to the resected vertebra, wherein the first dimension is selected from the group consisting of a resection angle (I.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the resected vertebra, a z offset (Z) between S1 and the center of the articulation radius, a facet angle (I.beta.) defining an orientation of the articulating surface, and IR.

169. The spinal implant kit of claim 168, wherein the first dimension comprises I.alpha. and the second dimension comprises Z.

170. The spinal implant kit of claim 169, wherein I.alpha. and Z are determined by measuring one or more of an x offset (IX) between S1 and a second pedicle saddle point (S2) of an adjacent vertebra, a y offset (IY) between S1 and S2, and a z offset (IZ) between S1 and S2.
and selecting first and second dimensions that are predetermined for one or more of a given IX value, a given IY value, and a given IZ value.

171. The spinal implant kit of claim 169, wherein I.alpha. ranges in magnitude from about 30° to about 70° and Z ranges from about 20mm to about 40mm.

172. The spinal implant kit of claim 164, further comprising a third prosthesis and a fourth prosthesis, each of which comprises a superior facet prosthesis, wherein each of the third and fourth prostheses is shaped to be attached to a second vertebra to replace a removed facet of the second vertebra by articulating against either of the first and second prostheses.

173. The spinal implant kit of claim 164, further comprising a third prosthesis and fourth prosthesis, each of which comprises a superior facet prosthesis, wherein each of the third and fourth prostheses is shaped to be attached to the vertebra to replace a second removed facet of the vertebra.

174. The spinal implant kit of claim 156, further comprising third, fourth, fifth, and sixth prostheses, each of which has a magnitude of the first dimension different from magnitudes of the first dimension of the remainder of the first, second, third, fourth, fifth, and sixth prostheses.

175. The spinal implant kit of claim 155, wherein the subset comprises multiple components that are shaped to be assembled together to form the selected prosthesis.

176. A spinal implant kit for replacement of a superior facet and an inferior facet of one or more vertebrae, the spinal implant kit comprising:
a plurality of superior facet prostheses, each of which is selectable to replace the superior facet, wherein each of the superior facet prostheses has a an articulating surface and a first dimension, wherein the first dimension varies in magnitude among the superior facet prostheses; and a plurality of inferior facet prostheses, each of which is selectable to replace the inferior facet, wherein each of the inferior facet prostheses has an articulating surface shaped to articulate against the articulating surface of any of the superior facet prostheses, and a second dimension, wherein the second dimension varies in magnitude among the inferior facet prostheses.

177. The spinal implant kit of claim 176, wherein the superior facet prostheses comprise a first superior facet prosthesis and a second superior facet prosthesis, wherein the first dimension varies in magnitude between the first and second superior facet prostheses.
wherein the inferior facet prostheses comprise a first inferior facet prosthesis and a second inferior facet prosthesis, wherein the second dimension varies in magnitude between tile first and second inferior facet prostheses.

178. The spinal implant kit of claim 177, wherein the superior facet prostheses further comprise a third superior facet prosthesis and a fourth superior facet prosthesis, wherein the first dimension varies in magnitude between the first, second, third, and fourth superior facet prostheses, wherein the inferior facet prostheses further comprise a third inferior facet prosthesis and a fourth inferior facet prosthesis, wherein the second dimension varies in magnitude between the first, second, third, and fourth inferior facet prostheses.

179. The spinal implant kit of claim 178, wherein the superior facet prostheses further comprise fifth, sixth, seventh, eighth, and ninth superior facet prostheses, wherein the inferior facet prostheses further comprise fifth, sixth, seventh, eighth, ninth, and tenth inferior facet prostheses.

180. The spinal implant kit of claim 176, wherein each of the superior facet prostheses has a third dimension that varies in magnitude among the superior facet prostheses independently of the first dimension, wherein each of the inferior facet prostheses has a fourth dimension that varies in magnitude among the inferior facet prostheses independently of the second dimension.

181. The spinal implant kit of claim 176, wherein the first dimension is selected from the group consisting of a resection angle (.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the vertebra, and a facet angle (.beta.) defining an orientation of the articulating surface.

182. The spinal implant kit of claim 181, wherein a and a vary in magnitude among the superior facet prostheses independently of each other.

183. The spinal implant kit of claim 182, wherein a ranges in magnitude from about 30° to about 70° and .beta. ranges from about 60° to about 100°.

184. The spinal implant kit of claim 176, wherein the articulating surface of each of the inferior facet prostheses comprises a center of an articulation radius, wherein each of the inferior facet prostheses further comprises an implant pedicle saddle point positioned to substantially overlie a pedicle saddle point (S1) of the vertebra when the inferior facet prosthesis is attached to the vertebra, wherein the second dimension is selected from the group consisting of a resection angle (I.alpha.) defining an orientation of a flat surface positioned to lie against a resection surface of the resected vertebra, and a z offset (Z) between S1 and the center of the articulation radius.

185. The spinal implant kit of claim 184, wherein I.alpha. and Z vary in magnitude among the superior facet prostheses independently of each other.

186. The spinal implant kit of claim 185, wherein I.alpha. ranges in magnitude from about 30° to about 70° and Z ranges from about 20mm to about 40mm.

187. A method for selecting a prosthesis of a spinal implant kit for replacing a natural facet of a vertebra of a spine, the spinal implant kit comprising a plurality of components, the method comprising:
measuring relative positions of a plurality of bony landmarks of the spine to obtain morphology data; and utilizing the morphology data to select a subset of the components of the spinal implant kit, the subset providing a selected prosthesis dimensioned to match a morphology of the vertebra.

188. The method of claim 187, wherein the subset is selected such that the selected prosthesis has an articulating surface that is positioned to approximate a position of the natural facet.

189. The method of claim 187, wherein the bony landmarks are selected from the group consisting a most medial and anterior point (P1) of an articulating surface of the natural facet, a most posterior and lateral point (P4) of the articulating surface of the natural facet, and a pedicle saddle point (S1) of the vertebra, wherein S1 defines an intersection between a posterior pedicle bone surface and a longitudinal axis of the pedicle, and a pedicle saddle point (S2) of an adjacent vertebra.

190. The method of claim 189, wherein the natural facet comprises a natural superior facet, wherein the selected prosthesis comprises a superior facet implant, wherein obtaining the morphology data comprises obtaining an offset between S1 and P1.

191. The method of claim 189, wherein the natural facet comprises a natural inferior facet.
wherein the selected prosthesis comprises an inferior facet implant, wherein obtaining the morphology data comprises obtaining an offset between S1 and S2.

192. The method of claim 189, further comprising forming a semispherical resection encompassing S1 to facilitate measurement of the relative positions of the bony landmarks.

193. The method of claim 187, wherein the plurality of components comprises a first prosthesis and a second prosthesis, each of which is of one-piece construction and is independently selectable to provide the selected prosthesis, wherein selecting a subset of the components comprises selecting one of the first prosthesis and the second prosthesis.

194. The method of claim 187, wherein the subset comprises multiple components, the method further comprising assembling the components of the subset together to from the selected prosthesis.