EP0502086A1 - Artificial hip-joint - Google Patents

Artificial hip-joint

Info

Publication number
EP0502086A1
EP0502086A1 EP91900393A EP91900393A EP0502086A1 EP 0502086 A1 EP0502086 A1 EP 0502086A1 EP 91900393 A EP91900393 A EP 91900393A EP 91900393 A EP91900393 A EP 91900393A EP 0502086 A1 EP0502086 A1 EP 0502086A1
Authority
EP
European Patent Office
Prior art keywords
joint
ball
socket
femur
titanium
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.)
Withdrawn
Application number
EP91900393A
Other languages
German (de)
French (fr)
Inventor
Bengt Persson
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.)
Volvo AB
Original Assignee
Volvo AB
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 Volvo AB filed Critical Volvo AB
Publication of EP0502086A1 publication Critical patent/EP0502086A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
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    • 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
    • A61F2/30721Accessories
    • A61F2/30734Modular inserts, sleeves or augments, e.g. placed on proximal part of stem for fixation purposes or wedges for bridging a bone defect
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    • 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
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    • 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
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    • A61F2/3601Femoral heads ; Femoral endoprostheses for replacing only the epiphyseal or metaphyseal parts of the femur, e.g. endoprosthetic femoral heads or necks directly fixed to the natural femur by internal fixation devices
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    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/74Devices for the head or neck or trochanter of the femur
    • A61B17/742Devices for the head or neck or trochanter of the femur having one or more longitudinal elements oriented along or parallel to the axis of the neck
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    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/84Fasteners therefor or fasteners being internal fixation devices
    • A61B17/86Pins or screws or threaded wires; nuts therefor
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    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30405Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by screwing complementary threads machined on the parts themselves
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    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30593Special structural features of bone or joint prostheses not otherwise provided for hollow
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    • 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
    • A61F2230/0063Three-dimensional shapes
    • A61F2230/0069Three-dimensional shapes cylindrical
    • 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

Definitions

  • the present invention relates to a hip joint or coxa prosthesis, comprising a joint socket with anchoring means for fixing the joint socket to a pelvic bone and a joint ball with anchoring means for fixing the ball to a sec-
  • the joint ball is joined to a long nail or a long ° pin of stainless steel or vitallium, inserted far into the central femural cavity and fixed therein by means of a two-component cement.
  • the nail or pin is subjected to great mechanical stress and fatigue fractures of the nail or pin are not uncommon. The fracture often occurs so far down in the central femoral cavity that it is not possible to reach the remaining portion of the pin from the end of the femur, in such a situation, the surgical method used to remove the pin end is to drill a hole from the side through the femur and partially into the pin.
  • the pin is thereafter chiselled upwards a short distance, whereafter a new hole is drilled into the pin, which is chiselled up another short distance. This procedure is repeated until the pin has been forced up sufficiently far to be able to be extracted from the exposed end of the femur. Surgical procedures of this type are time-consuming, taking up to five hours, and consequently involve severe stress on the patient and the surgical team. They are of course also costly.
  • the purpose of- the present invention is to provide a hip joint prosthesis, which is less susceptible to fracture due to fatigue, which makes it possible to more quickly and more simply than previously replace broken and worn components, and which also makes it possible to achieve in a simple manner exact fitting of the socket and ball to each other.
  • the anchoring means of the ball joint comprise a tubular element made of titanium designed to be received in a bone in the femur and be integrated with the femur, that the tubular element has an internally threaded bore and that when the element has been surgical ⁇ ly implanted, a screw is screwed into the bore and fixes the joint ball to the tubular element.
  • the basic difference between the invention and the pre- vious known technology is that the latter is based on cementing an anchoring element of a material which is not biocompatible, e.g. vitallium, in the femural cavity, while the present invention is based on the idea of using a biocompatible material such as titanium in the anchoring element and inserting the element into a bore axially to the neck of the femur, so that the anchoring element becomes integrated with the femur by new growth of bone tissue.
  • the tubular anchoring element which is preferably provided with internal threads, can then be used to fix the joint ball quite simply by screwing the ball or an intermediate wedge shaped element joined to the ball into the tubular element which is integral with the femur.
  • the wedge shaped element serves as a gauge block, and by vary ⁇ ing the wedge angle, the angle between the ball and the tubular anchoring means can be varied.
  • the socket can also be made with a socket-shaped carrier of titanium which is allowed to become embedded through bone growth in the pelvis, and the socket proper is then fixed therein.
  • Figure l shows schematically a portion of a pelvis and a femur with a partially sectioned hip joint prosthesis according to the invention in its integrated implanted state.
  • Figure 2 shows a view corresponding to that in Figure 1 of a prosthesis in a simpler embodiment
  • Figure 3 shows a fixture for cutting off the ball of the femur.
  • the numeral l in Figure l generally designates a portion of a pelvic bone and 2 designates the upper portion of a femur whih has been cut so that a flat sectional surface 3 has been formed.
  • the joint prosthesis has a socket 4 consisting of a bowl-shaped carrier 5 of titanium and a bowl-shaped polyethylene element 6 which forms the socket proper.
  • the carrier 5 is screwed into a cavity made in the pelvis by means of five titanium screws 7 (three shown). it has external grooves 8 on its surface facing the bone for integration therewith.
  • the ball 9 of the joint pros ⁇ thesis consists of a hemisphere 10 of titanium or stain ⁇ less steel and a titanium plate 11 which is wedge-shaped in longitudinal section.
  • an externally and internally threaded tube 12 is used to ⁇ gether with a screw 13 screwed into the tube, which screw is also screwed into a threaded bore 14 in the wedge shaped plate 11, which is made in one piece with a thread ⁇ ed stud 15, which is in turn screwed into a threaded bore in the hemisphere 10.
  • the wedge shaped plate 11 and the hemisphere 10 have interengaging grooves 16 and ridges 17 arranged coaxially with the stud 15 and being designed to remove some of the shear load from the screw fastening between the hemisphere 10 and the wedge plate 11.
  • Implantation of the joint described here is done by two operations at an interval between them of about four months, in the first surgical procedure, the bowl shaped titanium carrier 5 is screwed in place by means of screws 7 into the pelvis.
  • the socket 6 is replaced by a 2 to 3 mm thick polyethylene bowl in order to allow the screws 7 to become embedded.
  • a 16 mm diameter hole is also drilled in along the axis of the femoral head and the tube 12 is screwed into the hole.
  • the tube 12 has an internal thread along its entire length and perfora ⁇ tions 12a along approximately half its length, i.e. the portion which, when the components are assembled, lies beyond the screw 13.
  • the perforations are designed to provide the best possible anchoring in the femur through bone growth.
  • the 2 to 3 mm thick provisional polyethylene socket is replaced by the socket proper 6, which can consist of porous polyethylene with open pores and be impregnated with HEALON.
  • the bowl-shaped carrier 5 has an inwardly directed peripheral edge 5a, and the socket 6 is mounted in place by simply snapping it in behind the edge 5a.
  • a fixture 20 is used of the type shown in Figure 2.
  • the fixture consists of an arm 21 which is screwed into the lower end of the tube 12, a threaded stud bolt 22 screwed into the arm 21 and a plate 23 with a surface 24 parallel to the end 12b of the tube to be exposed by the cut, this surface 24 forming a reference plane in which the cut is made.
  • the threaded stud bolt 22 permits adjustment of the plate 23 to various distances from the arm 21, thus adapting it to tubes 12 of different lengths.
  • a wedge plate 11 is selected appropriate to the particular anatomy of the patient.
  • an assortment of wedge plates is available with wedge angles of at least between 15° and 25°.
  • the wedge angle is 20°.
  • Other parameters than the wedge angle can be varied to achieve optimum fit between the ball and the socket, e.g. the central axis of the stud 15 and the thickness of the wedge plate 11.
  • the wedge plate 11 is screwed securely against the cut surface 3 of the bone by means of the screw 13, which has a screwdriver groove at its lower end to permit final tightening of the wedge plate 11 against the bone surface 3.
  • the underside of the plate 11 in con ⁇ tact with the surface 3 is provided with teeth or grooves to promote integration with the bone.
  • the hemisphere 10 can be screwed onto the wedge plate 11 prior to or after the latter has been fixed to the tube.
  • the wedge plate has on one side a spherically curved surface lla, which forms a continuation of the surface of the hemisphere and provides an increased range of articulation.
  • Figure 2 shows a simpler model of a hip joint prosthesis. Details corresponding to those in Figure l have been given the same reference numerals as in Figure 1.
  • the prosthesis in Figure 2 differs from that described above in that there is no wedge. Instead, the ball 10 and the screw 13 are made in one piece. At the transition between the ball and the screw 13, there is a plate 30 with a smooth transition via a neck 31 to the ball 10. This embodiment ensures sufficient articulation.
  • the invention provides very secure anchoring of all of the components in the hip joint and at the same time provides easy replacement of components subject to wear, e.g. the polyethylene socket and the ball.

Abstract

Prothèse de l'articulation coxo-fémorale ou de la hanche composée d'un logement (5) et d'une rotule (10). Le premier est bouterollé dans un support de titane de forme creuse (5) solidement vissé au pelvis (3). La deuxième est fixée par une plaque cunéiforme (11) à un tube de titane fileté à l'intérieur et à l'extérieur (12) et vissé dans un trou situé dans l'axe de la tête et du col du fémur (2).Prosthesis of the hip joint or hip joint composed of a housing (5) and a ball joint (10). The first is bolted in a hollow titanium support (5) securely screwed to the pelvis (3). The second is fixed by a wedge plate (11) to a tube of titanium threaded inside and outside (12) and screwed into a hole located in the axis of the head and the neck of the femur (2) .

Description

ARTIFICIAL HIP JOINT
The present invention relates to a hip joint or coxa prosthesis, comprising a joint socket with anchoring means for fixing the joint socket to a pelvic bone and a joint ball with anchoring means for fixing the ball to a sec-
5 tional surface of a femur, the ball of which has been cut off.
In the majority of known hip joint prostheses of this kind, the joint ball is joined to a long nail or a long ° pin of stainless steel or vitallium, inserted far into the central femural cavity and fixed therein by means of a two-component cement. The nail or pin is subjected to great mechanical stress and fatigue fractures of the nail or pin are not uncommon. The fracture often occurs so far down in the central femoral cavity that it is not possible to reach the remaining portion of the pin from the end of the femur, in such a situation, the surgical method used to remove the pin end is to drill a hole from the side through the femur and partially into the pin. The pin is thereafter chiselled upwards a short distance, whereafter a new hole is drilled into the pin, which is chiselled up another short distance. This procedure is repeated until the pin has been forced up sufficiently far to be able to be extracted from the exposed end of the femur. Surgical procedures of this type are time-consuming, taking up to five hours, and consequently involve severe stress on the patient and the surgical team. They are of course also costly.
The purpose of- the present invention is to provide a hip joint prosthesis, which is less susceptible to fracture due to fatigue, which makes it possible to more quickly and more simply than previously replace broken and worn components, and which also makes it possible to achieve in a simple manner exact fitting of the socket and ball to each other.
This is achieved according to the invention in a hip joint prosthesis of the type described by way of introduction by virtue of the fact that the anchoring means of the ball joint comprise a tubular element made of titanium designed to be received in a bone in the femur and be integrated with the femur, that the tubular element has an internally threaded bore and that when the element has been surgical¬ ly implanted, a screw is screwed into the bore and fixes the joint ball to the tubular element.
The basic difference between the invention and the pre- vious known technology is that the latter is based on cementing an anchoring element of a material which is not biocompatible, e.g. vitallium, in the femural cavity, while the present invention is based on the idea of using a biocompatible material such as titanium in the anchoring element and inserting the element into a bore axially to the neck of the femur, so that the anchoring element becomes integrated with the femur by new growth of bone tissue. The tubular anchoring element, which is preferably provided with internal threads, can then be used to fix the joint ball quite simply by screwing the ball or an intermediate wedge shaped element joined to the ball into the tubular element which is integral with the femur. The wedge shaped element serves as a gauge block, and by vary¬ ing the wedge angle, the angle between the ball and the tubular anchoring means can be varied. By having available during the operation wedges with varying wedge angles, it is possible to achieve a very exact fit of the ball in the socket, in a corresponding manner, the socket can also be made with a socket-shaped carrier of titanium which is allowed to become embedded through bone growth in the pelvis, and the socket proper is then fixed therein.
The invention will be described below in more detail with reference to examples shown in the accompanying drawings, where
Figure l shows schematically a portion of a pelvis and a femur with a partially sectioned hip joint prosthesis according to the invention in its integrated implanted state.
Figure 2 shows a view corresponding to that in Figure 1 of a prosthesis in a simpler embodiment, and Figure 3 shows a fixture for cutting off the ball of the femur.
The numeral l in Figure l generally designates a portion of a pelvic bone and 2 designates the upper portion of a femur whih has been cut so that a flat sectional surface 3 has been formed. The joint prosthesis has a socket 4 consisting of a bowl-shaped carrier 5 of titanium and a bowl-shaped polyethylene element 6 which forms the socket proper. The carrier 5 is screwed into a cavity made in the pelvis by means of five titanium screws 7 (three shown). it has external grooves 8 on its surface facing the bone for integration therewith. The ball 9 of the joint pros¬ thesis consists of a hemisphere 10 of titanium or stain¬ less steel and a titanium plate 11 which is wedge-shaped in longitudinal section.
in order to fix the joint ball 9 to the exposed sectional surface 3 of the femur, according to the invention an externally and internally threaded tube 12 is used to¬ gether with a screw 13 screwed into the tube, which screw is also screwed into a threaded bore 14 in the wedge shaped plate 11, which is made in one piece with a thread¬ ed stud 15, which is in turn screwed into a threaded bore in the hemisphere 10. The wedge shaped plate 11 and the hemisphere 10 have interengaging grooves 16 and ridges 17 arranged coaxially with the stud 15 and being designed to remove some of the shear load from the screw fastening between the hemisphere 10 and the wedge plate 11. Implantation of the joint described here is done by two operations at an interval between them of about four months, in the first surgical procedure, the bowl shaped titanium carrier 5 is screwed in place by means of screws 7 into the pelvis. During the period of integrating bone growth, the socket 6 is replaced by a 2 to 3 mm thick polyethylene bowl in order to allow the screws 7 to become embedded. During the first operation, a 16 mm diameter hole is also drilled in along the axis of the femoral head and the tube 12 is screwed into the hole. The tube 12 has an internal thread along its entire length and perfora¬ tions 12a along approximately half its length, i.e. the portion which, when the components are assembled, lies beyond the screw 13. The perforations are designed to provide the best possible anchoring in the femur through bone growth.
in the second operation, the 2 to 3 mm thick provisional polyethylene socket is replaced by the socket proper 6, which can consist of porous polyethylene with open pores and be impregnated with HEALON. The bowl-shaped carrier 5 has an inwardly directed peripheral edge 5a, and the socket 6 is mounted in place by simply snapping it in behind the edge 5a.
Before the ball of the joint prosthesis with associated components is mounted on the tube 12, the head of the femur must be cut normal to the tube 12 and flush with the upper end of the tube. For this purpose, a fixture 20 is used of the type shown in Figure 2. The fixture consists of an arm 21 which is screwed into the lower end of the tube 12, a threaded stud bolt 22 screwed into the arm 21 and a plate 23 with a surface 24 parallel to the end 12b of the tube to be exposed by the cut, this surface 24 forming a reference plane in which the cut is made. The threaded stud bolt 22 permits adjustment of the plate 23 to various distances from the arm 21, thus adapting it to tubes 12 of different lengths. After the head of the femur is cut off, a wedge plate 11 is selected appropriate to the particular anatomy of the patient. Preferably, an assortment of wedge plates is available with wedge angles of at least between 15° and 25°. In the example shown in Figure 1, the wedge angle is 20°. Other parameters than the wedge angle can be varied to achieve optimum fit between the ball and the socket, e.g. the central axis of the stud 15 and the thickness of the wedge plate 11. The wedge plate 11 is screwed securely against the cut surface 3 of the bone by means of the screw 13, which has a screwdriver groove at its lower end to permit final tightening of the wedge plate 11 against the bone surface 3. The underside of the plate 11 in con¬ tact with the surface 3 is provided with teeth or grooves to promote integration with the bone. The hemisphere 10 can be screwed onto the wedge plate 11 prior to or after the latter has been fixed to the tube. As can be seen in Figure l. the wedge plate has on one side a spherically curved surface lla, which forms a continuation of the surface of the hemisphere and provides an increased range of articulation.
Figure 2 shows a simpler model of a hip joint prosthesis. Details corresponding to those in Figure l have been given the same reference numerals as in Figure 1. The prosthesis in Figure 2 differs from that described above in that there is no wedge. Instead, the ball 10 and the screw 13 are made in one piece. At the transition between the ball and the screw 13, there is a plate 30 with a smooth transition via a neck 31 to the ball 10. This embodiment ensures sufficient articulation.
The invention provides very secure anchoring of all of the components in the hip joint and at the same time provides easy replacement of components subject to wear, e.g. the polyethylene socket and the ball.

Claims

1. Hip joint or coxa prosthesis, comprising a joint socket with anchoring means for fixing the joint socket to a pelvic bone and a joint ball with anchoring means for fixing the ball to a sectional surface of a femur, the ball head of which has been cut off, c h a r a c t e r ¬ i z e d in that the anchoring means of the joint ball (10) comprise a tubular element made of titanium designed to be received in a bore in the femur and be integrated with the femur, that the tubular element (12) has an internally threaded bore and that, when the element has been surgically implanted, a screw is screwed into a bore and fixes the joint ball to the tubular element.
2. Joint prosthesis according to Claim 1, c h a r a c t - e r i z e d in that the screw (13) holds a titanium an¬ choring plate (11) which is wedge-shaped in longitudinal section against the sectional end surface of the femur, and that the ball (10) is fixed to the wedge shaped an¬ choring plate.
3. Joint prosthesis according to Claim 3, c h a r a c t ¬ e r i z e d in that the wedge-shaped element (11) and the ball (10) are joined to each other via a screw fastener (15) and have interengaging profiles (16, 17) designed to relieve the load of shear forces from the screw fastener.
4. Joint proshtesis according to Claim 1, c h a r a c t ¬ e r i z e d in that the screw fastener is formed by a threaded stud (15) joined to either the wedge shaped plate (11) or the ball (10), which stud is inserted into a threaded bore in the other one of said elements, and that interengaging grooves (16) and ridges (17) are arranged in the plate and ball coaxially about the stud and bore.
5. Joint prosthesis according to one of Claims 1-4, c h a r a c t e r i z e d in that the tubular element (12) is externally threaded and is intended to be screwed into the femur.
6. Joint prosthesis according to one of Claims 1-4, c h a r a c t e r i z e d in that the tubular element (12) is perforated over that portion of its length which, when the wedge shaped anchoring plate (11) is screwed in place, lies beyond the inserted screw (13).
7. Joint prosthesis according to one of Claims 1-6, c h a r a c t e r i z e d in that the socket (4) has components (5) consisting of titanium which are intended to be integrated with the pelvic bone.
8. Joint prosthesis according to Claim 7, c h a r a c t ¬ e r i z e d in that the socket comprises a titanium socket (5) intended to be screwed securely to and inte- grated with the pelvic bone, and that a polyethylene socket shaped lining (6) is fixed to the titanium socket.
9. Joint prosthesis according to Claim 8, c h a r a c t ¬ e r i z e d in that the titanium socket (5) has inwardly directed edges (5a) behind which the socket shaped lining is snapped.
10. Device for use in cutting off the head of a femur during surgical implantation of a hip joint prosthesis in accordance with one of Claims 1-9, c h a r a c t e r ¬ i z e by a support (21) which can be fixed to the free end of the tubular titanium element (12), which support is joined to a fixture (23) via setting means (22), by means of which the fixture can be set co-planar with the inner tube end (12b).
11. Device according to Claim 10, c h a r a c t e r ¬ i z e d in that the support (21) is an arm (21) which can be screwed securely to the free end of the tubular element (12), that the setting means comprise an elongated element (22) directed parallel to the tubular element and which can be fixed to the support (21) in various positions, and that the fixture is formed by a plate (23) carried by said arm and having a surface (24), which by means of the setting means can be set co-planar with the inner tube end (12b).
EP91900393A 1989-11-30 1990-11-30 Artificial hip-joint Withdrawn EP0502086A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8904053 1989-11-30
SE8904053A SE8904053L (en) 1989-11-30 1989-11-30 HOEFTLEDSPROTES

Publications (1)

Publication Number Publication Date
EP0502086A1 true EP0502086A1 (en) 1992-09-09

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Country Status (4)

Country Link
EP (1) EP0502086A1 (en)
JP (1) JPH04503181A (en)
SE (1) SE8904053L (en)
WO (1) WO1991007932A1 (en)

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Also Published As

Publication number Publication date
JPH04503181A (en) 1992-06-11
WO1991007932A1 (en) 1991-06-13
SE8904053L (en) 1991-05-31
SE8904053D0 (en) 1989-11-30

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