CA1112805A - Joint prosthesis - Google Patents

Joint prosthesis

Info

Publication number
CA1112805A
CA1112805A CA316,296A CA316296A CA1112805A CA 1112805 A CA1112805 A CA 1112805A CA 316296 A CA316296 A CA 316296A CA 1112805 A CA1112805 A CA 1112805A
Authority
CA
Canada
Prior art keywords
pivot member
prosthesis
components
securing means
joint prosthesis
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA316,296A
Other languages
French (fr)
Inventor
Leonard J. Schwemmer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lord Corp
Original Assignee
Lord Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lord Corp filed Critical Lord Corp
Priority to CA379,598A priority Critical patent/CA1125453A/en
Priority to CA379,599A priority patent/CA1124452A/en
Application granted granted Critical
Publication of CA1112805A publication Critical patent/CA1112805A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/42Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes
    • A61F2/4241Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/50Prostheses not implantable in the body
    • A61F2/60Artificial legs or feet or parts thereof
    • A61F2/66Feet; Ankle joints
    • A61F2/6607Ankle joints
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
    • A61F2002/30138Convex polygonal shapes
    • A61F2002/30154Convex polygonal shapes square
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30563Special structural features of bone or joint prostheses not otherwise provided for having elastic means or damping means, different from springs, e.g. including an elastomeric core or shock absorbers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/50Prostheses not implantable in the body
    • A61F2002/5007Prostheses not implantable in the body having elastic means different from springs, e.g. including an elastomeric insert
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0002Two-dimensional shapes, e.g. cross-sections
    • A61F2230/0017Angular shapes
    • A61F2230/0021Angular shapes square
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00017Iron- or Fe-based alloys, e.g. stainless steel
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00023Titanium or titanium-based alloys, e.g. Ti-Ni alloys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00029Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T403/00Joints and connections
    • Y10T403/32Articulated members
    • Y10T403/32606Pivoted
    • Y10T403/32614Pivoted including circumferential biasing or damping means
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T403/00Joints and connections
    • Y10T403/45Flexibly connected rigid members
    • Y10T403/454Connecting pin traverses radially interposed elastomer

Abstract

ABSTRACT OF THE DISCLOSURE
A joint prosthesis comprises two relatively in-extensible primary components that are spaced apart from one another. Disposed between and spaced from both of the com-ponents is a pivot member. The pivot member is resiliently secured to each of the primary components so as to permit-relative rotation between the primary components and the pivot member. As a result, the two primary components of the prosthesis can rotate toward and away from each other about an axis that is disposed at least adjacent to and at least approximately parallel to a central longitudinal axis of the pivot member. The pivot member and the primary components of the prosthesis are preferably secured together by one or more bodies of elastomer.

Description

1~28~5 elated ApPlications The present application describes, illustrates, and claims joint prostheses 15 that are similar .n strutture and operation to joint ~rostheses described, illus^
trated, and claimed in two commonly owned, concurrently filed applications of James B. Koeneman, entitled "Knee Joint Prosthesis" and "Joint Prosthesis ~lth Contoured Pin", and in a commonly owned, concurrently ~iled joint application of Leonard J. Schwemmer and Howard T~ Wilson, entitled "Ar~le Joint Prosthesis".
Rac~round of the Invention ~ esilient materials, such as elastomers, have long been used in external prosthetic devices or the human body to cushion impact or shoclc loads. Because r ~L ~L128r~S

impact loads are necessarily and regularly encountered ln walking, two common prosth~tic devices that have often incorporated resilient materials are artificial fe~t a~ ankle joint prostheses for use with artificial feet. In early designs, an ankle joint prosthesis was typically a metallic pivot that included a plain (e. g,, 5 sleeve) bearing or a rolling element (e. g,, ~all) bearing. Resilient or elastomeric ma$eri3~ was disposed both about the pivot to help limit its motion and in various portions of an associated artificial foot to cushion or absorb im.pact loads. Typical combinations of a cushioned artificial foot and an ankle joint prosthesis that in-corporates a metal-on-metal pivot are described and illustrated in Ehle U. S.
Patent~o, 487,697, R~wleyU, S. PatentNo, 1,090,881, andKaiserU, S. Patent No. 2, 183,076, Later in the development of ankle joint prostheses for external use, resilient or elastomeric material came to be utilized i~r properties other th~n its ability to absorb or cushion impact loads, In Desoutter U. S, Patent No, 1,911,440, for example, a tubular rubber bushing is secured between a pin and a metal sleeve that circumscribes the pin to form a pivot for an ankle joint prosthesis. The outer sleeve is connected to an artificial foot, while the pin is connected to an artificial lower leg. Articulation is permitted by torsional de-flection of the bushing. Because of the resilience of the bushing material, the 20 ankle joint prosthesis automatically returns to a preselected position after it is deflected. The prosthesis also does not require lubrication because the bushing separates the adjacent metal surfaces of the pin and the sleeve. Similar ankle joint prostheses that employ a tubular bushing or body of elastomer between an outer rigid sleeve and an inner pin or sleeve are described and illustrated in BurgeretalU. S. PatentNo. 2,~05,475andPrahlU. S. PatentNo, 3,480,972, ~128~5 A pivot or pivotable assembly that incorporates a relatively thin, tubular body o~ elastomer secured between a pin and a larger diameter sleeve is only capable of extensive pivotal or rotational movement about a single aYls. In a typical ankle joint prosthesis, such as the Desoutter and Prahl prostheses, 5 such an elastomeric pivot is oriented generally perpendicular to the longitudinal axis OI the wearer's leg and trans~7erse to the longitudinal axis of the wearer's artifici21 foot. In the orient tion that has been described, the elastomeric pivot permits extensive flexion in the dorsal and plantar directions. An elastomeric pi~Tot so oriented, howe~er, can only prwide a limited degree of inversion and 10 eversion of a foot about its longitudinal axis or a parallel axis and only a limited degree of internal and external rotation of the foot about the longitudinal axis of ihe leg. The motions other than flexion are all accommodated primarily through co~npression o~ the e;astomeric bushing, which is relatively thin and cannot affor~ any significant degree of deflection. To overcome some of the motion 15 limitations inherent in the ankle joint prostheses of the Desoutter and Prahl pstents, the ankle joint prosthesis of the previously mentioned Burger et al patent incorporates two elastomeric pivots disposed at right angles to each other. The Burger et al ankle joint prosthesis thus can resiliently permit both extensive dorsal and plantar flexion and extensive inversion and e~7ersion Cther external ankl e 20 joint prostheses attempt to provide the three types of movement afforded by a natural ankle joint through the use of relatively massive blocks of elastomer, rather than the tubular bushings discussed above The blocks OI elastomer may be specially shaped or contoured in order to provide appropriate sti~înesses or motion capabilities in the three critical rctational directions. EY~amples of ex-25 ternal ankle joint prostheses that inc~rporate la ge blocks of elastomer aredescribed and illustrated in Bennington et al U S Patent No. 2,692,392 and Asbelle et al U S Patent No 3,982,280 ~128¢:! 5 Although resilient materials, and particularly elastomeric materials, have for many years been suggested for use in external joint prostheses, the useof resili~nt or elastomeric materials in internal joint prostheses has only recently been proposed The apparent delay in the appearance of proposals for the use OI
resilient or elastomeric materials internally of the human body is probably at-tributabl~ in part to the lack of a physiologically inert elastomeric material that could safely be used in the body. Nonetheless, with the development of suitable elastomeric materials, such as Dow Corning Corporation's Silastic~' silicone elasto~Ler, a number of surgically implantable, elastomeric joint prostlleses have been proposed, particularly for finger joints. The finger joint prostheses, in particular, tend to be entirely formed of elastomer or nearly so Unfortunatel~, such designs reqllire the elastomer to be bent or fLexedextensively at some point to provide a pivot. The result is alternating tension and compression loading of the elastomer, which is detrimental to its long-term ~atigue life The use of notches in the elastomer to locate the pivot point further adds to the ~tresses in the elastomer. Examples of finger joint prostheses that are entirely formed of elastomer or nearly so are described and illustrated in Swanson U. ~. Patent No 3, 462, 7~5~ Niebauer et al U S. Patent No. 3, 593, 342, Lynch U. S. Patent No 3,881,786, andSwansonU S. PatentNo. 3,875,594. Ctherthanthefinger;oint prostheses mentioned above, relatively few implantable prostheses that employ resilient or elastomeric material have been identified. Nonetheless, the use of elastom~ric material in an implantable hip joint prosthesis is suggested in Buechel etal U S. Patent No. 3,916,451, particularly Figure 1, and in Bokros etalU 3 PatemNo 3,707,006, particularlyFigure5 The ankle joint prostheses described in the previously mentioned patents to Desoutter, Burger et al, and Prahl appèar to represent the best presently known designs for use of the desirable properties of elastomeric material in a 111281`~"5 prosthesis that accomrnodates pivotal or rotational motion Nonetheless, the elastom~ric pivots that are incorporated in the ankle joint prostheses of these three patents do not make optimal use of elastomeric material within the space provide~ In particular, the relatively thin, tubular bodies of elastomer in the ankle joint prostheses of Desoutter, Burger et al, and Prahl are subjected to relatively high, torsionally-induced strains which, over periods of extended use, will lead to failure of the elastomeric bodies. While the strains experienced bythe elastomeric bodies of the patented ankle joint prostheses may not be detri-mental in terms of a few hundred or even a few thousand articulations of the prostheses, the strains are critical when one considers several million articulations or deflections of the prostheses. Such numbers of articulations may easily be experienced during a year or two OL normal use. In an a~le joint prosthesis that is used externally of the human body, replacement of the elasto-meric elements of the prosthesis may merely represent additional expense and - s~me inconvenience to the user If such a joint prosthesis were impl~nted in the body of the user, on the other hand, failure of the elastomeric elements within one or two years would seriously limit the desirability of using such a prosthesis Summary of the Invention The present invention is directed to a joint prosthesis which is suitable for either internal or external use and which is constructed resiliently to per~nit and accommodate pi~70tal or rotational movement, with a view to providing maximum useful life. A joint prosthesis according to the invention comprises a pair of primary components that are formed of relatively inextensible material and are spaced apart from one another Disposed between and spaced from each of the two components is a pivot member that is also formed of relatively inextensible ~Z8~

m~terial, The pivot member is resiliently secured to each of the prim~ry com-ponents so as to permit and accommodate relative rotation between the pivot mernber and the com~onents, As a result, the two primary components of the prosthesis can rotate toward and away from each other about an air.is that is - disposed at least adjacent to and at least approximately parallel to a central axis of the pivot member. 'Ihe use of a pivot member and a pivot aY.is that are separate from the primary components of a joint prosthesis permits the prosthesis to have, Ior e~ample, a relatively small size for a given angular motion to be accommodated and a given maximum strain in the material that resiliently secures the pivot member to the primary components. Alternatively, the prosthesis of the present invention will permit, for a given angular motion to be accommodated and a given size of the prosthesis, a lower maximum strain in and a larger service life ~or the resilient material that secures together the pivot member and the primary components of the prosthesis, The foregoing !~ advantages are experienced particularly with reference to a prosthesis such as th~ prostheses of Desouttèr U. S. Patent No. 1,911,440 and Prahl U. S. Patent No, 3, 480, 972, in which the pivot member or pin is rigidly secured to one of the primary components of the prosthesis, In a preferred embodiment of the invenhon, the pivot member is secured
2~ to the primary components of the prosthesis by a member that is at least partially ~ormed of elastomer. Attachment of the pivot member to the primary components only through a member or body that is resilient in whole or part will insure that the prosthesis is free of any relatively inextensible, and hence motion re-straining, connection between the primary components, The resilient securing ~5 member will typically include a first portion that secures th~ pivot member to one of the primary components of the prosthesis and a second portion that secures the pivot member to the other primary component of the pr~sthesis, The two :L11;28~5 portion~ of the resilient securing member are preferably arcuately shaped wh~n viewed in section taken generally normal to the central longitudinal axis of the pivot member. Each of the first and second portions of the securin~ member will also preferably include a pair of exposed surfaces that eY.tend generally 5 length~rise of the pivot member and outwardly from adjacent the pivot member.
The exposed surfaces of one portion of the resilient securing member are spaced apart from the exposed surfaces of the other portion of the securing member throughout at least a majority of their respective len~ths measured generally radially of the pivot member. Such a spacing between the two portions 10 of the resilient securing member facilitates relative pivo'al motion or rotation between the pivot member and either of the primary components of the prosthesis without interference from the other primary component of the prosthesis or its associated portion of the securing member. Also to facilitate relative pivotal motion or rotation, each of the primary components of the prosthesis will 15 preferably include a surface that is concavely arcuate in shape when viewed in section taken generally normal to the central longitudinal axis of the pivot member Each of the arcuate surfaces of the primary components is presented to and spaced from a convexly arcuate surface o;f the pivot member. At least one of the two primary com~onents of the prosthesis should include structure for attaching 20 the component to a limb associated with the human body When the present invention is embodied in an external ankle joint prosthesis, for example, the securing member that includes two portions which resiliently secure the primary components of the prosthesis to the pivot member also includes a portion secured to at least one of the primary eomponen s at a 25 pOillt behind an arcuate surface of the component which is presented to the pivot member. This third portion of the securing member extends from the primary component to which it is attached toward the other primary component of the i ~;28`~5 prosthesis resiliently to limit relative rotation between the two primary com-ponents, particularly relative rotation between the rear portions of the primarycomponents, The resilient securing member may al:,o include a fourth portion that is secured to at least one of the two primary components of the prosthesis at a point in front of the arcuate surface of the component which is presented to the pivot member, The fourth portion of the securing mernber extends from the component to which it is secured toward the other primary component of the prosthesis, With such an orientation, the fourth portion of the securing member resiliently lirnits relative rotation between the front of one primary componentand the front of the other primary component. Each of the third and fourth portions of the securing member should be at least partially formed of elastomer, The opposed surfaces of the two primary components of the ankle joint prosthesis should each include an arcuately shaped portion presented to the pivot member of the prosthesis, a portion disposed in front of the arcuate portion, and a portion 1~ disposed to the rear of the arcuate portion, The front portions of the opposed surfaces of the two primary componen's should be disposed to diverge from one another in a direction away from the pivot member. The rear portions of the two opposed surfaces should be similarly disposed, Brief Description of the Drawin~s For a better understanding of the invention, reference may be made to the following description of several exemplary embodiments, taken in conjunctionwith the figures of the accompanying drawings, in which:
Figure 1 is a side view of an ankle joirlt prosthesis according to ',he invention mounted between an artificial leg and an artificial foot;

Figure 2 is a plan view, partly in section, of the joint prosthesis oî
~igure 1, taken along line 2-2 of Figure 1;
Figure 3 is a side view, on an enlarged scale, of the ankle joint prosthesis of Figure 1;
Figure 4 is a side view of a second ankle joint prosthesis according to the invention;
Figure 5 is a plan view of the joint prosthesis of Figure 4;
~igure 6 is a side view, in section, of another embodirnent of an ankle joint prosthesis according to the invention;
Figure 7 is a side vie~ of yet another embodiment of an an~le joint prosthesis according to the invention;
Figure 8 is a sectional view of the ankle joint of Figure 7, taken along line 8-8 of Figure 7; and ~gure 9 is a perspective view of an endoprosthetic finger joint according to the invention.

Descriptlon of Embodiments ~gure 1 of the drawings illustrates, in side view, an ankle joint prosthesis 10, according to the present invention, mounted between an artificial lower l ~g12 and an artificial foot 14. The artificial leg 12 may be formed of any one of a number of materials that have the strength necessary to support the weight of the human body, such as metal, wood9 nylon~ or reinforced pLastic. The leg 12 is hollow and includes a generally tubular body portion 16 and an end wall 18 that is d~sposed adjacent the prosthesis 10. The end wall 18 is formed with an opening 20 which extends a~nally of the leg 12 and which receives and fixedly mounts a nut 22. Screwed into the nut 22 is the threaded stud 24 of a metal mounting adapter 26, The adapter 26 includes both the threaded stud 24 and a circular base plate _ 9 _ .

28 from one side of which the stud projects in a direction perpendicuLar to the plane of the base plate. As best shovJn in Fi~ure 2, the hase plate 28 has four circum~Qrentially spaced apart holes formed in it. ~,ach of the holes in the base B plate 2~ receives a screw 34 that is screwed into an upper surface of the ankle joint prosthesis 10 to secure the mounting adapter 26 to the prosthesis. A second metal rnounting adapter 30, which is, but need not be, identical to the adapter 26, is secured to a lower surface of the prosthesis 10 opposite the surface to whichthe adapter 26 is secured. Four screws (not shown) are received in holes formed in the base plate 32 of the adapter 30 and are screwed into the prosthesis 10. Athreaded stud 34, which is immovably connected to the base plate 32, extends perpendicularly away from the plane of the base plate and into an opening 36 formed vertically through tne artificial foot 14 just forward OI the heel of the fo~t. The openinu 36 in tne foot 14 receives and fix~dly mounts a nut 38 into which the threaded stlld 34 is screwed. 171e artificial foot 14, like the artificial leg 12, is formed Gf a mate~ial, such as metal, wood, nylon, or reinforced plastic, that is strong enough to support the weight of the human body. In addition, the material of which the foot 14 is formed should also afford some resilience or give. Resilence OI
the foot will attenuate, to some extent, the shock loads imposed on the foot andtransmitted from the foot through the ankle jOil t prosthesis 10 and the artificial leg 12 to the user's body when the foot stri~.es a hard surface, as in walking.
Additional resilience may be provided by incorporating within the artificial foot 14 one or more bodies of elastomer or other resilient material A typical artificial îoot t~t incorporates several discrete bodies of elastomer disposed to provide additi~nal resilience is described and illustrated in Kaiser U S Pa'.ent No.
2, 183,076.
The ankle joint prosthesis 10 incorporates two identical and vertically spaced apart primary components 40 and 42. Each of the primary components 40 and 42 is formed of a relatively inextensible material, such as met~l, pl~stic, or reinforced plastic The material of which the primary components 40 and 42 are formed must be suitable for bonding to elastomer, for reasons that 1llill be-come apparent, and is to be judged as to its relative inei~ter~ibility through 5 comparison to the elastomer utilized in the prosthesis 10. The components 40 and 42 incorporate contoured surfaces 44 and 46J respectively, which are presented toward, but spaced apart from each other. Cpposite their respective contoured surfaces 44 and 46, the components 40 and 42 nave generally planar surfaces 48 and 50, respectively, The planar surface 48 of the component 40 is present~d 10 to and juxtaposed with the surface of the adapter base plate 28 opposite the stud B 24. The screws ~that are received in the holes in the base plate ~ are screwed into threaded, blind bores (not shown) formed in the surface 48 and the component ~.0 ~ a similar manner, the planar surface 50 of the component 42 is presented to and juxtaposed with the surface of the adapter base plate 32 opposite the stud 15 34. The screws ~not shown) that are received in the holes ~not shown) in the base plate 32 are screwed into threaded, blind bores (not shown) formed in the planar surface~and the component 42. Although the primary components 40 and 42 of the prosthesis 10 are attached to separate mounting adapters 26 and ~, re-spectively, the studs 24 and 34 of the adapters could each be formed in one piece 20 with an adjacent primary component.
The contoured surface 44 of the primary component 40 of the prosthesis 10 includes a central portion 52 that is concavely arcuate in shape, when viewed from the side, as in F~gure 1. To the rear of its central porticn 52, the surface 44 includes a planar rear portion ~4 that slopes toward the surface 48 from front 2~ to rear of the prosthesis 10. In front of its central portion 52, the surface 44 includes a planar front portion 56 that slopes toward the surface 48 from rear to front of the prosthesis 10 The contoured surface 46 of the component 42 similarly includes a concavely arcuate central portion 58, a planar rear portion Gn~ and a ~Z8i~5 s~c~
r C~ planar front portion 62 The front and rear portions 62 and 60 of the surface 4~
slope toward the surface 50 Disposed between the spaced apart arcuate portions 52 and 58 of the contoured surfaces 44 and 46 is a cylindrical pivot member or pin 64. The pin 64 is forrned of a relatively inexte~sible material, such as metal, reinforced plastic, or nylon, and is oriented such that its central longitudinala~ns 66 is generally perpendicular to the longitudinal axis of the leg 12 and transversely disposed relative to the longitudinal axis of the Ioot 14. Because OI
its shape and orientation, the pin 64 presents a convexly arcuate surface to each of the arcuate surface portions 52 and 58 of the prim~ry components 40 and 42, respectively, of the prosthesis 10. The pin 64 is resiliently secured to the com-ponents 40 and 42 of the prosthesis 10 by a body or mass of resilient materiaL
68, such as elastomer. The elastomer in the mass 68 may be natural rubber or a synthetic ~lastomer. Although all of the resilient material in the prosthesis 10 is part of a single interconnected mass 68, each of the various portions or 5 sections of the n~ss 68 which are described hereinafter m~y be formed as a discre~e member if such a procedure appears desirable for manufacturing or other purposes.
The convexly arcuate, outer circumferential surface of the pin 64 is resiliently secured to the arcuate surface portion 52 of the component 40 by an arcuately shaped portion 70 of the resilient or elastomeric mass 68. When viewed in section taken normal to the longitudinal axis 66 of the pln 64, the elastomeric portion or section 70 resembles a truncated wedge taken from an annulus. The elastomeric section 70 is bonded, by vulcanization or adhesives, for example, to both a portion of the convexly arcuate outer surface of the pin C ~ / ~C~ ~ c~o~ 2 ~5 64 and to the ~eEally ~ portion 52 of the surface 44 To secure the pin 64 to the other primary component 42, a similar arcuately shaped portion or ~128~5 section 72 of the mass o elastomer 68 is disposed between and bond~d to a B portion of the convexly arcuate outer surface of the pin~and to lhe concavely arcuate surface portion 58 of the component 42. The elastomeric sections 70 and 72 include pairs of exposed surfaces 74 and 76, respectively, that e~tend lengthwise of the pin 64 and outwardly, in a generally radial direction, from the outer circurnferential surface of the pin. Throughout most of their lengths,as measured radially of the pin 64, the exposed surfaces 74 of the elastomeric section 70 are spaced apart fromthe exposed surfaces 76 of the elastomeric section 72. The surfaces 74 do intersect the surfaces 76 adjacent the pin 64, but diverge ~romthe surfaces 76 with increasing radial distance from th~- pin~
a similar manner, the front planar portion 56 of the contoured surface 44 of the component 40 diverges from the front planar portion B2 of the contoured surface 46 of the component 42. The rear portions 54 and 60 of the surfaces a4 and 46 also diverge with increasing radial distance from the pin 64. As a resultof the aivergence between the surfaces 74 and 76 and between the surface portions 56 and 62 and 54 and 60, there can be relative pivotal or rotational movement between the pin 64 and the primary component 40, for example, with-out interference between the elastomeric section 70 that will be deflected to accomnodate such relative rotation and the el~.,tomeric section 72 and without interference between the two prirnary components 40 and 42 of the prosthesis 10.The elastomeric portions 70 and 72 of the mass of elastomer 68 in the prosthesis 10 will resiliently permit and, to a limited extent, resiliently resist relative rotation between the pin 64, on the one hand, and the primary components 40 and 42, on the other hand Rotational or pivotal motion that corresponds to 2~ dorsal or plantar fle~on of a natural ankle joint will occur about an axLs that is disposed at least adjacent to and at least approximately parallel to the longitudinal ~1~2BQ5 axis ~S6 of the pin 64. Although the elastomeric sections 70 and 72 v~ill offer some resiliGnt resistance to dorsal and plantar ~exion, the elastorner will be loadedin torsional shear and will not offer sufficlent resistance to fle;~.ion to cushion and li~it this motion, Thus, secured to the rear portions 54 and 60 of the con-toured surfaces 44 and 4~ of the components 40 and 42 are rear elastomeric bumFer portions 78 and 80, respecti~ely, of the elastomeric mass 68. Each of the rear bumpers 78 and 80 extends away from thesurface portion 54 or 60 to which the bumper is secured and toward the other rear bumper. Nonetheless, the rear bumpers 78 and 80 are separate from each other and are spaced slightly apart when the prosthesis 10 is in its normal undeflected position, Conseque~tl~, no tension load will be applied to either of the bumpers 78 and 80, when, for e}~m~le, relative rotation between the primary components 40 and 42 of the pros~esis 10 causes the rear portions 54 and 60 of the surfaces a4 and 46 to move away from each other. The ankle joint prosthesis 10 also includes front bumLers 82 and 84 that are portions of the mass of elastomer 68 incorporated in the prosthesis, The front bumpers 82 and 84 are secured to front portions 56 and 62, respectively, o~ the contoured surfaces 44 and 46 of the primary com-r ponents 40 and 42. Each of the bumpers 82 and 84 extends away from the ~rurfac^
l~t~ 0~
~ ~to which lt is secured and toward the other front bumper, Like the rear bumpers 78 and 80, the bumpers 82 and 84 are not joined together so that no tension loads can be imposed on the bumpers 82 and 84, when, for example, relative rotation between the components 40 and 42 of the prosthesis 10 causes ~e surface portions 56 and 62 to move away from eaGh other, As should be apparent, the bumpers 78, 80, 82, and 84 will resist flexion of the prosthesis 10 through compression loading o~ the elastomer in the ~umpers, The operation of the ankle joint prosthesis 10 will be described with the ll~Z~
user or wearer extending the artificial leg 12 and foot 19 to take a ~tep Ac t~le heel of the artificial foot 14 strikes the ground, the rear of the primary om-ponent 40 of the prosth~sis io rotates toward the rear of the ~rimarSr omponent 42 about the axis 66 of the pin 64. The elastomeric portions 70 and 72 that secure the components 40 and 42 to the pin 64 deflect in torsional shear to permit the relative rotation that occurs between the primary components and the pin. At the same time, the rear bumpers 78 and 80 come together and are compressed to Iimit tne rotational movement and to help absorb the impact load imposed on the foot 14. As the weight of the user or wearer of the prosthesis 10 comes forward on the prosthesis and the foot 14, the rear of the component 40 begins to rotateaway from the rear of the component 42. The rotation relieves the torsional deflection of the elasto~eric por~ons 70 and 72 and the compression loads on the bumpers 78 and 80. As the wei~ht of the user and the leg 1~ continue to m~e forward, the elastomeric portions 70 and 72 are again deflected in torsional shear ~nd the front bumpers 82 and 84 come together and are compressed so as to limit relative movement of the front of the component 40 toward the front of the component 42. When the user lifts the artificial foot 14 from the grolmd, ashe prepares to take another step, the loads on the bumpers 82 and 84 and the elastomeric portions 70 and 72 are relieved.
. The primary motion that the prosthesis 10 is desi~ned to accommodate is dorsal and plantar flexion of the foot 14 with respect to the artificial leg 12.Flexion occurs about an axis disposed generally perpendicular to the longitudinal axis of the leg 12 and transverse to the longitudinal axis of the foot 14 or, inother words, about an a~ns that is at least adjacent to and at least appro~mately 26 parallel to, if not coincident with, the longitudinal axis 66 of the pin 64. Coin-cidence between the axis of rotation and the axis 66 will depend, in part, on ~h~ pin ~S~
B whether the pin 64 shifts during rotation between~t and a primary component 40 - ~5 -~lZ~3Q5 ~, or 42 Incorporation of resilient material into the prosthesis 10 al~.o permits the prosthesis to accommodate lirnited degrees of internal and e~ternal rotation, as well as inversion and eversion, of the artificial foot 1~1. To permit inversion and eversion of the ~oot 14, which is rotation about an a;~.is generally parallel to 5 the lon~itudinal axis of the foot, the primary components 40 and 42 of the prosthesis 10 mus t rotate toward each other adjacent one or the other of the two sides of the prosthesis. The rela~ve rotation between the components 40 and 42 is accom-modated by compression of the two elastomeric por~ons 70 and 72 adjacent one side of the prosthesis 10 or one end of the pin 64. Adjacent the other side of the prosthesis 10 and the other end of the pin 64, the elastomeric portions 70 and 72 may be placed in tension as the primary components 40 and 42 rotate away from each other Alternatively, the weight of the user or wearer of the prosthesis 10 may impose a sufIicient compressive preload on the elastomeric portions 70 and 72 so that the relative rotation of the components 40 and 42 away from each other merely relieves the preload without impcsing tension loads.
Ex~ernal and internal rotation of the foot 14, which occurs about an axis that is generally parallel to, if not coincident with, the longitudinal axis of the leg 12, is accommodated primarily through shearin~ de~lection of the elastomeric portions 70 and 72. Because of the spaces between the exposed surfaces 74 and 76 of the elastomeric portions 70 and 72, respectively, and because of the spacing between the primary components d~0 and 42, there is essentially no compression of elastomer required to accommodate rotation of the foot 14 Consequently, external and internal rotation is accomplished more easily or with less force than inversicn or eversion. If the prosthesis 10 is unable to provide a sufficient de~ree of rotation, a supplemental rotator may be used with the prosthesis Such a ~11;28'Q5 rotator Nould be disposed between the upper prirnary cornponent 40 of the prosthesis 10 and the artificial lower leg 12, for e~ample. I~pical supplementalrotators are described and illustrated in Moore U. S. PatentNo. 3,95~,775, H~upt U. S. Patent No. 4,007,497, and Cwens et al U. S. Pat~nt No. 4,038,70~.
~lthough the ankle joint prosthesis 10 of ~igures 1 and 2 may be perceived as having a structure that is similar to the structure of the ankle joint prosthesis shovm in Prahl U. S Patent No. 3, 480, 972, for example, there is a difference in structure that is significant in terms of the useful service life of the two prostheses In the Prahl ankle ioint prosthesis, and in similar prostheses, a tubular bushing of elastomer is disposed between and bonded to a rigid outer sleeve and an inner pin. The sleeve is attached to an artificial lower leg, for example, while the pin is attached to an artificial foot, for example. Flexion beh~een~ the foot and the leg is accommodated b~ torsional deflection of the elasto-meric bushing The degree of the resulting strain in the elastomer of the bushingwill depend upon the radial thickness of the bushing and the a~ount of rotational or torsional motion that must be accommodated. For a given amount of torsional motion, a relatively thin elastom~ric bushing will experience relatively high strains and will provide a relatively short ser~ice life because of early fatigue failure of the elas omer. A thicker bushing will reduce the strains experienced by the elastomer and provide improved service life, but will also probably in-crease the overall size of the prosthesis. In addition, the effective spring rate of an element of elastomer at any distance from a point about which pi~ otal motionoccurs is proportional to the spring rate of the elastomer in translational shear multiplied by the square of the distance from the pi~ot point. Since the elastomer that is closest to the pivot point is effectively much softer in rotational shear than elastomer that is farther from the pivot point, the major portion of the torsior~al 1S.~28~5 strain or deflection in an elastomeric bushing, for example, will occur in the elastomer that is closest to the pivot point. Consequently, doubling the radial thic~.ness of an elastomeric bushin~ vJillnothalve the rna;~imum strains e;~-perienced by the elastomer as it deflects to perrnit pivotal motion, but will have a much smaller effect on red~.lcing the strains.
The prosthesis 10 affords a more efficient and effective method of con-trolling strains in its constituent mass of elastomer 68 because the rotational motion that is necessitated by flexion between the leg 12 and the foot 14 is accom-modated by two distinct portions 70 and 72 of the elastomeric mass which are disposed at equal distances from the aYls of pivotal motion. Approx rnately halfof the rotational motion between the primary components 40 and 42 of the prosthesis 10 which is required by flexion between the foot 14 and the leg 12 is~ccommodated by deflection of the elastomer 70 between the pin 64 and the com-ponent 40 The other half of the motion is accommodated by deflection of the elasto~ier 72 betv~een the pin 64 and the primary component 42 of the prosthesis10. Thus, for the same diametral dimensions, the prosthesis 10 will effectively provide twice as much motion accommodation for a given maximum strain or half as much strain for a given degree of flexion as will a prosthesis constructed such as the one shown in the Prahl patent ~ggures 4 and 5 of the application drawings illustrate another embodiment 10' of the ankle joint prosthesis 10 shown in Figures 1, 2 and 3. In Figures 4 and 6, elements of the prosthesis 10' that correspond to elements of t~,e prosthesis 10 are designated with corresponding, but primed reference numerals. The prosthesis10', ~i~;e the prosthesis 10, includes a pair of spaced apart, primary components 401 and 42' that are fabricated of a relatively nonextensible material. Each of the primary components 40' and 42' includes a contoured surface 44' or 46' and an '~

~L128QS

opposed planar surface 48' or 50', Disposed between concavely arcuate portions 52' and 58' of the contoured surfaces 44' and 46' is a cylindrical pin 64' that is formed of a relatively ineYtensihle material. Elastorneric elernents 70' and 72'secure the pin 64' to the components 40' and 42', respectively Cne difference between the prosthesis 10' and the prosthesis 10 is that a single, one-piece rear bumper 86 is disposed between the components gO' and 42' of the prosthesis 10', unlike the separate rear bumpers 78 and 80 of the prosthesis 10. The one-piece rear bumper 86 facilitates molding of the elastomeric portions of the prosthesis 10' by eliminating the need $o m~intain a narrow space between two separate rear bumpers. In addition, the one-piece construction eliminates the possibility that dirt and grit will be introduced between two separate bumpers and thereafter abrade and wear the elastomer in the bumpers The bumper 86 may, however, be subjected to tension loads during operation of the prosthesis 10' to accommodate fle~on. As previously discussed, tension loads aredetrimental to the fatigue life of an elastomeric member, particularly when the tension loads alternate with compression loads, as would be the case with the bumper 86. Nonetheless, the bumper 86 will also be subjected to a compressive preload that results from the weight of the user of the prosthesis The compres-sive preload will c ' least minimize, and perhaps totally eliminate, what would otherwise be tension loads on the bumper 86 as the prosthesis 10' flexes to bring the front portions of the primary components 40' and 42' of the prosthesis toward each other. The possibility of tension loads on the one-piece rear bumper 86 will also be reduced because the front portions 56' and 62' of the contoured surfaces44' an~ 46', respectively, of the prosthesis components 40' and 42' are relatively close togetber, as compared to the corresponding surfaces 56 and 62 in the prosthesis 10. Thus, the plantar fLexion of which the prosthesis 10' is capable is significantly less than the flexion of which the prosthesis 10 is capable Another difference between the prosthesis 10' and the prosthesis 10 is that the primary components 40' and 42' of the prosthesis 10' have roughly octagonal shapes in plan view, as shown in Figure 5, as opposed to the rectan-gular shapes of the components 40 and 42 of the prosthesis 10. As should be apparent from Figure 2, the octangonal shapes of the components 40' and 42' eliminate the corners of the components 40 and 42 which project beyond the side surfaces or outline of the upper portion of the foot 14. The prosthesis 10' alsoincludes relatively prominent grooves 88 formed in the surface of the rear bumper 86 adjacent the interfaces between the bumper and the primary com-ponents 40' and 42'. The grooves 88 tend to relieve the high stresses that mightotherwise occur at the interf~ces. The pin 64' includes a blind bore 90 in each end to facilitate locating the pin in its proper orientation and position in a mold for forming the elastomeric portions of the prosthesis 10'. Projections in the mold are provided to engage the blind bores 90 and hold the pin 64' in place during transfer and curing of the elastomer.
Yet another e~bodiment 10" of the present invention is illustrate~ in section in Figure 6, As with the ankle joint prosthesis 10' of Figures 4 and 5, double primed reference numerals are used in i~'igure 6 to designate elements ofthe prosthesis 10" that correspond to similarly referenced elements of the prosthesis 10. Cne difference between the ankle joint prosthesis 10" and the prosthesis 10 of Figures 1 and 2 is the incorporation into the prosthesis 10" of a one-piece rear bumper 92, similar to the one-piece rear bumper 88 of the prosthesis 101. The rear bumper 92 is not formed wholly of elastomerj however, but includes a shim 9~ formed of a relatively nonextensible material, such as me~l or reinforced plastic. The shim 94 will theoretically reduce the ability of ~ L~128~5 the elastomer in the bumper 92 to bulge under compressive loads. Consequently, as compared to a similar bumper without a shim, the bumper 92 should be able to support a substantially greater load for a given outward bulge or vertical deflection. The use of one or more shims 94 is a method of increasing the com-5 pression stiffness or spring rate of the rear bumper 92 without utilizing a typeor grade of elastomer in the rear bumper that is different from the elastcmer used elsewhere in the prosthesis A problem with using the shim 94, however, is that there is a definite tendency for the shim to displace outwardly from the elastomer by movin~ to the left as viewed in Figure 6, thereby defeating the 10 intended purpose of the shim. A possible solution to the problem is taper the shim 94 such that the thickest portion of the shim is closest to the pin 64.
The ankle 30int prosthesis 10" of Figure 6 incorporates a rotator 98 to supplement the capabiliiy of the basic prosthesis struciure to accommodate in-ternal and external rotation The supplemental rotator 96 includes a cylindrical body of elastomeric material 98 in which are embedded three annular shims 100 that are fabricated of relatively nonextensible material. As with other components of the prosthe.aes 10, 10' and 10", the elastomeric material 98 may be natural or synthetic rubber, while the inextensible material may be metal, reinforced plastic, or any other material which will bond to the elastomer 98 and which is 20 relatively inextensible as compared to the elastomer. The rotator 96 is received in a recess 102 formed in the planar upper surface 48 " of the primary component 40" of the prosthesis 10" Placing the rotator 96 in the recess 102 decreases the extent to which the rotator 96 increases the total height of the prosthesis 10".
The elastomer 98 in the rotator 96 is bonded, at ~ne end, to the surface 48" of the component 40" at the bottom of the recess 102 and, at the other end, to a supplemental plate 104. The plate 104 is spaced from the upper surface 48" of ~ 1~2~S
the ~rirnary prosthesis component 40" and is provided with tr~o threaded bores 106. The bores 106 will accept screws (not shown) for securing the prosthesis 10"
to an element such as a mounting adapter or an artificial lov~er leg. In operation, the rotator 96 will permit internal and external rotation of a foot through torsional shearing of the elastomer 98. The shirns 100 will reduce the tendency of ths rotator 96 to deflect under the weight of a user's body.
To guard against tension loads in the elastomer of both the rotator 96 and the rear bumper 92, a member 108 that is flexible, but relatively inex-tencible, such as a wire cable, extends between the lower primary component 42" of the prosthesis 10" and the supplemental plat~o 104 at the upper end of the prosthesis. The cable 108 is received in a bore 110 which is formed vertically through the center of the prosthesis 10" and which h~s a diameter sufficiently greater than the outer diameter of the cable to perrnit the prosthesis to function without interference from the cable. Buttons 112 at each end of t~e cable 108 hold the cable in place in the primary component 42" and the supplemental plate 104 of the prosthesis 10'1, The amount of compressive preload thatis tobe applied to th~ elastomeric elements of the prosthesis 10" will determine the amount of tension to be imposed on the cable 108" It would be possible to provide for ad-justment of tension in the cable 108 during use of the prosthesis 10" by providing a threaded engagement between the buttons 112 and the cable, as suggested by Asbelle etal U. St Patent No 3,982l280.
A fourth embodiment of an an~le joint prosthesis 10"' of the present in-vention is shown in Figures 7 and 8, As with the prostheses 10' and 10" of F~gures 4 and 5 and Figure 6, respectively, elements of the prosthesis 10"' of Figures 7 and 8 corresponding to elements of the prosthesis 10 of Figures 1 and 2 are designated with ~}e same reference numerals as the elements of the ~128~5 prost~:esis 10, but with a triple-prime superscript. Generally speaking, the le joint prosthesis 10"' closely resembles the an~le joint prosthesis 10' o~
~igur~s 4 and 5 . There are two significant differences, one cf which is the addition of curved shims 114 of nonextensible material to the portions 70"' and 72"' OI the elastomeric mass 68"' which secure the pin 64"' to the primary com-ponents 40"' and 42"' of the prosthesis 10"'. The shims 114 will increase the compr~ssion load carrying capability o~ the prosthesis lO'i' without significantly interf-ring ~nth its ability to accommodate rotational motion of the components 40"' and 42"' of the prosthesis about the longitudinal axis of the pin 64"', for e~m?le. Another significant difference between the prosthesis 10"' and the prosthesis 10' is that the pin 64"' is arcuate in shape not only in planes normal to its longitudinal central axis 66"' but also in planes that are parallel to and exten d throug;~ the longitudinal axis of the pin, as best shown in Figure 8. The arcuate ~(~B portions 52"' and 58"' o~cont~ur~ ,~facc~ 4~ a..d ~ oî the primary com-ponents 40"' and 42"7, respectively, are also curved în two perpendicular planes, as are the shims 114. The result of the double curvature of the outer surface of the pin 64"' and the corresponding surfaces of other elements in the prosthesis 10"' will be an increased ability of the prosthesis 10"' to accommodate inversion and eversion, as compared to the prostheses 10, lC' and 10".
~o . Although all of the foregoing embodiments of the invention have been ankle joint prostheses intended for use externally of the human body, the basic pivot structure that is incorporated in each of the foregoing embodiments of the in-vention may also be utilized in a joint prosthesis intended for use internally of the body Figure 9 of the drawings illustrates a finger joint prosthesis 116, for 25 e~m?le, that incorporates two opposed and spaced apart primary components 118 and 120. The primary components 118 and 120 are formed of a relatively inextensible and physiolagically inert material, such as titaniumJ stainless steel, ~ 112~ 5 cobalt~hromium alloys, nylon, silicone resins, or high density polyethylene.
The components 118 and 120 include head portions 122 and lZ4, respectively, and shank or stem portions i26 and 128, respectively. The head portio~s 122 and 124 are each fixed to one end of their respective stem portions 126 and 128,5 which are relatively long and tapered to facilitate insertion into the intramedullary canals of the finger bones. The stem portions 126 and 128 of the components 118 and 120, respectively, will typically be cemented in place in their respective finger bones and m~y have specially contoured outer surii3ces to improve the attachment to the bones. Alternatively, or additionally, the stem portions 126 10 and 128 may be coated with or formedfrom a porous material into which boney tissue may grow to secure the primary components 118 and 120 of the prosthesis 116 to their respective finger bones.
The head portions i22 and 124 of the primary components 118 and 120 of the prosthesis 116 include surfaces 130 and 132, respectively, that are arcuate in at le~st one plane. The concavely arc~late surfaces 130 and 132 of the head por~ons 122 and 124 are presented generally toward each other and are spaced apart from each other. Interposed bet~7een and spaced fromeach of the arcuate surfaces 130 and 132 is a cylindrical pin 134. The pin 134 is secured to the surface 130 by a body of resilient material 136 md to the surface 132 by a similar body of resilient material 138. Each of the bodies of resilient material 136 and 138 is preferably formed of an elastomer that is physiologically inert.
When viewed in section taken normal to the central longitudinal a~ns 140 of the pin 134, each of the bodies of resilient material 136 and 138 resembles a truncated wedge. The curved base of each wedge~ ;e body of resilient material 13G or 138 is bonded to a corresponding arcuate surface 130 or 132 of a component 118 or 120, while the curved, truncated apex of the resilient body 136 or 138 is bonded to the 286~5 convex.ly arcuate outer surface of the pin 134. The bodies of resilient mat~rial136 and 138 are bonded to the outer circumference of the pin 134 at approximately opposit~ locations and have pairs of exposed surfaces 142 and 144, respectively,that ext~nd lengthv~ise of the pin 134 and outwardly fromadjacent the circumference of the pin, The exposed surfaces 142 of the body of resilient rnaterial 136 are spaced apart from the exposed surfaces 144 of the body of resilient material 138along all of their respective lengths measured in a generally radial direction outward from the pin 134.
~ operation, the finger joint prosthesis 116 ~nctions in much the same m~nner as the ankle joint prosthesis 10 of Figures 1 and 2. For example, fLexionbetween adjacent bones in the finger into which the prosthesis 116 is implanted causes relative rotation between the pin 134 and one or both of the primary com-ponents 118 and 120 about an axis that is at least adjacent to and at least approx-imately parallel to the longitudinal axis 140 of the pin, The motion is resiliently permitted and accommodated through torsional deflection of the bodies of resilient material 136 and 138. The motion limiting effects provided by the front and rear bumpers 78, 80, 82, and 84 in the external an~le joint prosthesis 10 shown in Figures 1 and 2, for example, are provided for the prosthesis 116 by the ~nuscles, tenc~ns, and ligaments of the finger into which the prosthesis is implanted. The muscles and tendons will normally not be destroyed or rendered inoperative by the implantation procedure, Pivotal motions between the ~lnger bones into which the prosthesis 116 is implanted which correspond to inversion and eversion and internal and external rotation of a foot will be accommodated primalily ~y compression and shearing, respectively, of the re~ilient bodies 136and 138.
Although the bodies of resilient material 136 and 138 are illustrated as being ~Iholly formed of elastomer, it woulcl be possible to incorporate into theresilient bodies shims of nonextensible material, as was done in the ankle jointprosthesis 10"' of Figures 7 and 8. It is unlikely, hov~ever, that the compressive loads on the bodies of resilient material 136 and 138 in the finger joint prosthesis 116 vJill be of such a magnitude to require the addition of shims. Similarly, the pin 134, the bodies of resilient material 136 and 138, and the arcuate surfaces 130 and 132 of the prosthesis 116 might be curved both in planes that are normalto the longitudinal axis 140 of the pin and in planes that are parallel to the longi-~dinal axis and pass through the axis, as with the pin 64"' of Figure 8. In a finger joint prosthesis for a proximal interphalangeal joint, the additional motion accommodation associated with such a double curvature is probably not required.
Cn the other hand, in prostheses for other joints of the body, such as metacarpal-phala~geal joints or shouLder joints, double curvature of the various componentsof the prostheses may be desirable to provide additional motion accommodation The additional motion accommodation may also be afforded by shortening the ~r length of the pin 134, for example, or by increasing the thicknesses of the bodies of resilient material 136 and 138, as ~neasured generally radialLy of the- pin 13~. Conversely, lengthening the pin 134 or decreasing the thicknesses OI
the resilient bodies 136 and 138 will decrease the motion accommodation tha.
is afforded about axes other than the axLs 140 or an adjacent, parallel axis Such structural adjustments to alter the motion accommodation characteristics of the prosthesis 116 may also be used in the prostheses 10, 10', 10" and 10"' and in similar prostheses for replacernent of other body joints In this reg~rd, although thc illustrated embodiments of the invention are an ankle joint for ex- -25 ternal use and a finger joint for internal use, the prosthesis of the invention is sui~ble as an external or internal replacement for both an ankle joint and a finger 11128~5 joint and for other joints in the body, including shoulder joints, hip joints, elbow joints, and knee joints. In some joint prostheses, pivot members or pins that are curved in more than one plane may be a distinctadvantage, if not a necessity.
As should be apparent from the various Figures of the drawings, the spacing between the two elastomeric sections that secure the pin to the primary components of each prosthesis may vary considerably. In the prosthesis 116 of Figure 9, for example/ the exposed surfaces 142 and 1~4 of the resilient bodies 136 and 138 are widely spaced apart, even at their closest points. In the prosthesis 10" of Figure 6, on the other hand, the exposed surfaces 74" and 76" of the elastomeric sections 70" and 72", respectively, are relatively close together, particularly in the front of the prosthesis. It would be possible and acceptable, moreover, for the elastomeric sections 70" and 72", for example, to be completely inter-connected and form a continuous annulus. The disadvantage of using a continuous annulus is that relative pivotal motion ~-0 between the primary components of a prosthesis would req~lire -both torsional shearing and compression of the elastomer as soon as the motion began. Because any body of elastomer naturally has a compression modulus that is three or more times its shear modulus, the requirement for immediate compression loading would mean that pivotal motion would be more difficult to accommodate or, in other words, would require more actuating force.
It will be understood that the embodiments described above are merely exemplary and that persons skilled in the art may make many variations and modifications without departing from the spirit and scope of the invention. All such modifications and variations are intended to be within the scope of the in-vention as defined in the appended claims.

Claims (20)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A joint prosthesis comprising (a) a first relatively inextensible component; (b) a second relatively inextensible component that is spaced from the first component along a first axis; (c) means defining a relatively inextensible pivot member disposed between and spaced from each of the first and second components, the pivot member having a center and a central axis which passes through said center and which is oriented generally perpendicular to said first axis, the first and second components being disposed entirely on opposite sides of and separated by a plane oriented generally perpendicular to said first axis and generally parallel to said central axis of the pivot member; and (d) means for resiliently securing the pivot member to each of the first and second components, the securing means including (i) a first portion that secures the pivot member to the first component, and (ii) a second portion that secures the pivot member to the second component, each of the first and second portions of the securing means having at least one exposed surface that extends outwardly from adjacent the pivot member, said at least one exposed surface of the first portion of the securing means being spaced from said at least one exposed surface of the second portion of the securing means throughout at least a majority of their respective lengths measured generally radially of said central axis of the pivot member, the first and second components being coupled to each other only through the pivot member and the first and second portions of the securing means, the relative extensibil-ity of the first and second components and the pivot member being determined in comparison to the securing means, the securing means resiliently permitting and accommodating relative rotation between the pivot member and the first component and between the pivot member and the second component so that the first and second components can move toward and away from each other in directions generally parallel to said first axis through rotation about a second axis that is disposed at least adjacent to and at least approximately parallel to the central axis of the pivot member.
2. A joint prosthesis, according to claim 1, wherein the pivot member is connected to each of the first and second components only through the securing means.
3. A joint prosthesis, according to claim 1, wherein the prosthesis is free of any substantially inextensible connection between the first and second components.
4. A joint prosthesis, according to claim 1, wherein at least one of the first and second components includes means for attaching said at least one component to a limb associated with a human body.
5. A joint prosthesis, according to claim 1, wherein the securing means is at least partially formed of elastomer.
6. A joint prosthesis, according to claim 5, wherein each of the first and second portions of the securing means is at least partially formed of elastomer.
7. A joint prosthesis, according to claim 6, wherein the first and second portions of the securing means are arcuately shaped when viewed in section taken generally normal to the central axis of the pivot member.
8. A joint prosthesis, according to claim 7, wherein each of the first and second portions of the securing means has a pair of exposed surfaces, each exposed surface extending generally lengthwise of the pivot member and outwardly from adjacent the pivot member, the exposed surfaces of the first portion of the securing means being spaced from the exposed surfaces of the second portion of securing means throughout at least a majority of their respective lengths measured generally radially of the central axis of the pivot member.
9. A joint prosthesis, according to claim 1, wherein each of the first and second components includes a surface that is concavely arcuate in shape when viewed in section taken generally normal to the central axis of the pivot member, each of the arcuate surfaces of the first and second components being presented to and spaced from a convexly arcuate surface of the pivot member.
10. A joint prosthesis, according to claim 9, wherein each of the concavely arcuate surfaces of the first and second components is parallel to the convexly arcuate surface of the pivot member to which said each concavely arcuate surface is presented.
11. A joint prosthesis, according to claim 1, wherein the central axis of the pivot member is disposed between and spaced from each of the first and second components.
12. A joint prosthesis comprising (a) a first relatively inextensible component having a first arcuate surface; (b) a second relatively inextensible component that is spaced from the first component along a first axis, the second component having a second arcuate surface spaced from the first arcuate surface; (c) means defining a relatively inextensible pivot member that is disposed between and spaced from each of the first and second components, the pivot member having a center and a central axis which passes through said center and which is oriented generally perpendicular to said first axis, the first and second components being disposed entirely on opposite sides of and separated by a plane oriented generally perpendicular to said first axis and generally parallel to said central axis of the pivot member, the pivot member also having at least one arcuate surface and each of the first and second arcuate surfaces being presented to and spaced from an arcuate surface of the pivot member; and (d) means for resiliently securing the pivot member to each of the first and second components, the securing means including (i) a first portion which is at least partially formed of elastomer and which secures the pivot member to the first arcuate surface and (ii) a second portion which is at least partially formed of elastomer and which secures the pivot member to the second arcuate surface, each of the first and second portions of the securing means having at least one exposed surface that extends outwardly from adjacent the pivot member, said at least one exposed surface of the first portion of the securing means being spaced from said at least one exposed surface of the second portion of the securing means throughout at least a majority of their respective lengths measured generally radially of said central axis of the pivot member, the first and second components being coupled to each other only through the pivot member and the first and second portions of the securing means, the relative extensibility of the first and second components and the pivot member being determined in comparison to the elastomer of the securing means, the first and second portions of the securing means resiliently permitting and accommodating relative rotation between the pivot member and each of the first and second components so that the first and second components can move toward and away from each other in directions generally parallel to said first axis through rotation about a second axis that is disposed at least adjacent to and at least approximately parallel to the central axis of the pivot member.
13. A joint prosthesis, according to claim 12, wherein the pivot member is connected to the first and second components only through the first and second portions of the securing means.
14. A joint prosthesis, according to claim 12, wherein at least one of the first and second components includes means for attaching said at least one component to a limb associated with a human body.
15. A joint prosthesis, according to claim 12, wherein each of the first and second portions of the securing means has a pair of exposed surfaces, each exposed surface extending generally lengthwise of the pivot member and outwardly from adjacent the pivot member, the exposed surfaces of the first portion of the securing means being spaced from the exposed surfaces of the second portion of the securing means throughout at least a majority of their respective lengths measured generally radially of the central axis of the pivot member.
16. A joint prosthesis according to claim 12, wherein each of the first and second surfaces is concavely arcuate and said at least one arcuate surface of the pivot member is convexly arcuate.
17. A joint prosthesis, according to claim 16, wherein each of the first and second arcuate surfaces is disposed parallel to an arcuate surface of the pivot member.
18. A joint prosthesis, according to claim 12, wherein said at least one arcuate surface of the pivot member and each of the first and second surfaces is arcuately shaped when viewed in section taken generally normal to the central axis of the pivot member.
19. A joint prosthesis, according to claim 12, wherein the pivot member is cylindrical in shape, and wherein the central axis of the pivot member is a central longitudinal axis of the pivot member.
20. A joint prosthesis, according to claim 13, wherein the central axis of the pivot member is disposed between and spaced from the first and second components.
CA316,296A 1977-11-16 1978-11-15 Joint prosthesis Expired CA1112805A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CA379,598A CA1125453A (en) 1977-11-16 1981-06-11 Joint prosthesis
CA379,599A CA1124452A (en) 1977-11-16 1981-06-11 Joint prosthesis

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US852,183 1977-11-16
US05/852,183 US4229839A (en) 1977-11-16 1977-11-16 Joint prosthesis

Publications (1)

Publication Number Publication Date
CA1112805A true CA1112805A (en) 1981-11-24

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CA316,296A Expired CA1112805A (en) 1977-11-16 1978-11-15 Joint prosthesis

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US (1) US4229839A (en)
JP (1) JPS5478894A (en)
CA (1) CA1112805A (en)
DE (1) DE2849588C2 (en)
GB (1) GB2008410B (en)

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Also Published As

Publication number Publication date
JPS5478894A (en) 1979-06-23
DE2849588A1 (en) 1979-05-17
US4229839A (en) 1980-10-28
GB2008410A (en) 1979-06-06
DE2849588C2 (en) 1984-08-23
GB2008410B (en) 1982-08-04
JPH0133174B2 (en) 1989-07-12

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