FR2977791A1 - Implant i.e. scapula implant, for articulation prosthesis of shoulder, has articular part provided with groove that is arranged in wall delimiting periphery of conical cavity, where groove emerges from cavity - Google Patents

Implant i.e. scapula implant, for articulation prosthesis of shoulder, has articular part provided with groove that is arranged in wall delimiting periphery of conical cavity, where groove emerges from cavity Download PDF

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Publication number
FR2977791A1
FR2977791A1 FR1156282A FR1156282A FR2977791A1 FR 2977791 A1 FR2977791 A1 FR 2977791A1 FR 1156282 A FR1156282 A FR 1156282A FR 1156282 A FR1156282 A FR 1156282A FR 2977791 A1 FR2977791 A1 FR 2977791A1
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FR
France
Prior art keywords
implant
groove
cavity
articular
conical
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.)
Granted
Application number
FR1156282A
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French (fr)
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FR2977791B1 (en
Inventor
Jean-Jacques Martin
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.)
FX SHOULDER SOLUTIONS, FR
Original Assignee
Compagnie Financiere et Medicale SAS
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Application filed by Compagnie Financiere et Medicale SAS filed Critical Compagnie Financiere et Medicale SAS
Priority to FR1156282A priority Critical patent/FR2977791B1/en
Publication of FR2977791A1 publication Critical patent/FR2977791A1/en
Application granted granted Critical
Publication of FR2977791B1 publication Critical patent/FR2977791B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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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
    • A61F2/40Joints for shoulders
    • A61F2/4081Glenoid components, e.g. cups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • 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
    • A61B17/80Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates
    • A61B17/8052Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates immobilised relative to screws by interlocking form of the heads and plate holes, e.g. conical or threaded
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • 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
    • A61B17/84Fasteners therefor or fasteners being internal fixation devices
    • A61B17/86Pins or screws or threaded wires; nuts therefor
    • 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
    • A61F2/30721Accessories
    • A61F2/30749Fixation appliances for connecting prostheses to the body
    • 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
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2/4603Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
    • A61F2/4612Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof of shoulders
    • 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
    • A61F2002/30143Convex polygonal shapes hexagonal
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    • 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
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    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30332Conically- or frustoconically-shaped protrusion and recess
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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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    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30332Conically- or frustoconically-shaped protrusion and recess
    • A61F2002/30349Conically- or frustoconically-shaped protrusion and recess the male and female complementary cones being of different conicities, i.e. for reducing the contact area
    • 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
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30332Conically- or frustoconically-shaped protrusion and recess
    • A61F2002/3035Conically- or frustoconically-shaped protrusion and recess the male convex cone having an inner female concave taper
    • 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
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30362Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit with possibility of relative movement between the protrusion and the recess
    • A61F2002/30364Rotation about the common longitudinal axis
    • A61F2002/30367Rotation about the common longitudinal axis with additional means for preventing said rotation
    • 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
    • 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
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30476Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements locked by an additional locking mechanism
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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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
    • A61F2/02Prostheses implantable into the body
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    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
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    • A61F2002/30772Apertures or holes, e.g. of circular cross section
    • A61F2002/30774Apertures or holes, e.g. of circular cross section internally-threaded
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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
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    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30795Blind bores, e.g. of circular cross-section
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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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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    • A61F2/30Joints
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    • A61F2002/3082Grooves
    • AHUMAN NECESSITIES
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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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    • A61F2/30771Special 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
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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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    • A61F2/30771Special 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
    • A61F2002/30879Ribs
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    • 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
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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
    • 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

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  • Health & Medical Sciences (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Prostheses (AREA)

Abstract

The implant (1) has a base plate (2) for osseous anchoring, and an articular part (3) forming an articular joint surface (4), where the articular part includes a conical cavity (16), and the base plate includes a male conical part or a head (5). The male conical part is inserted into the conical cavity until complete wedging takes place. The articular part is provided with a groove (17) that is arranged in a wall delimiting a periphery of the conical cavity, where the groove emerges from the cavity.

Description

La présente invention concerne un implant faisant partie d'une prothèse d'articulation, notamment un implant d'omoplate faisant partie d'une prothèse d'articulation de l'épaule. Une prothèse d'articulation de l'épaule comprend, de manière bien connue, un implant huméral, incluant une tige médullaire destinée à être insérée dans le canal médullaire de l'humérus, et un implant d'omoplate destiné à être fixé au niveau de la cavité glénoïdale de l'omoplate, cette tige médullaire et cet implant d'omoplate étant aptes à coopérer l'un avec l'autre par des surfaces articulaires complémentaires respectives qu'ils forment. The present invention relates to an implant forming part of a joint prosthesis, in particular a scapula implant forming part of a shoulder joint prosthesis. A shoulder joint prosthesis comprises, in a well known manner, a humeral implant, including a medullary stem intended to be inserted into the medullary canal of the humerus, and a scapula implant intended to be fixed at the level of the glenoid cavity of the scapula, the medullary stem and scapula implant being able to cooperate with each other by respective complementary joint surfaces they form.

L'implant d'omoplate est dans certains cas monobloc mais est fréquemment formé par l'assemblage d'une embase d'ancrage osseux et d'une pièce articulaire formant la surface articulaire. Cette surface articulaire peut être concave, pour la constitution d'une prothèse dite "anatomique", ou peut être convexe, pour la constitution d'une prothèse dite "inversée". Dans ce deuxième cas, la pièce articulaire est fréquemment dénommée "glénosphère" en référence à sa forme hémisphérique, et l'embase d'ancrage osseux est fréquemment dénommée "métaglène". L'assemblage de la pièce articulaire à l'embase d'ancrage osseux est fréquemment réalisé par l'aménagement dans l'un de ces deux éléments d'une cavité conique à faible pente et, dans l'autre élément, une partie conique mâle à pente correspondante, cette partie conique mâle étant destinée à être insérée dans la cavité conique jusqu'à coincement. Avec ce type d'implant existant, il apparaît que la résistance de l'assemblage des deux éléments l'un à l'autre peut ne pas être suffisante pour supporter les efforts répétés exercés sur l'implant d'omoplate par certains mouvements de la personne appareillée. La présente invention a pour objectif de remédier à cet inconvénient essentiel. Un autre inconvénient de ce type d'implant existant est le risque d'un positionnement angulaire défectueux de la pièce articulaire par rapport à l'embase d'ancrage osseux, ce qui est gênant lorsque la partie d'assemblage que comprend cette pièce articulaire est désaxée par rapport à un axe passant par le centre de la partie articulaire que forme cette pièce articulaire. La séparation de deux éléments dont l'assemblage est défectueux peut être particulièrement difficile et longue à réaliser. The scapula implant is in some cases monobloc but is frequently formed by the assembly of a bone anchor base and an articular part forming the articular surface. This articular surface may be concave, for the constitution of a so-called "anatomical" prosthesis, or may be convex, for the constitution of a so-called "inverted" prosthesis. In this second case, the joint piece is frequently called "glenosphere" with reference to its hemispherical shape, and the bone anchoring base is frequently referred to as "metaglene". The assembly of the articular part to the bone anchoring base is frequently achieved by the arrangement in one of these two elements of a conical cavity with a low slope and, in the other element, a male conical part. corresponding slope, this male conical portion being intended to be inserted into the conical cavity until jamming. With this type of existing implant, it appears that the strength of the assembly of the two elements to one another may not be sufficient to withstand the repeated forces exerted on the scapula implant by certain movements of the paired person. The present invention aims to overcome this essential disadvantage. Another disadvantage of this type of existing implant is the risk of a defective angular positioning of the articular part relative to the bone anchoring base, which is troublesome when the assembly part that comprises this joint piece is offset with respect to an axis passing through the center of the articular portion that forms this articular part. The separation of two elements whose assembly is defective can be particularly difficult and time consuming.

La présente invention a également pour objectif de remédier à cet inconvénient important. L'implant concerné. Selon l'invention, l'élément comprenant ladite cavité conique présente au moins une rainure aménagée dans sa paroi délimitant la périphérie de cette cavité conique, cette rainure débouchant dans cette cavité. L'inventeur a en effet découvert qu'une telle rainure permettait d'augmenter d'environ 20 % la résistance en traction de l'assemblage de la pièce articulaire à l'embase d'ancrage osseux, et d'augmenter d'environ 30 % la résistance en torsion de ce même assemblage, permettant ainsi d'obtenir une résistance d'assemblage pleinement suffisante pour supporter les efforts répétés exercés sur l'implant d'omoplate par certains mouvements de la personne appareillée. Les pentes respectives de ladite cavité conique et de ladite partie conique mâle pourraient être identiques ; de préférence, toutefois, elles sont différentes l'une de l'autre, de 3 à 10 minutes d'angle, ce qui, en combinaison avec ladite rainure, permet d'obtenir un assemblage parfaitement résistant de la pièce articulaire à l'embase d'ancrage osseux. Cette différence de pente est de préférence de 5 minutes d'angle, et, selon une forme de réalisation de l'invention dans ce cas, la pente de ladite cavité conique est de 5°45' et celle de ladite partie conique mâle est de 5°40'. Les éléments peuvent être en tous matériaux implantables appropriés. En particulier, la pièce articulaire peut être en alliage de chrome et de cobalt et l'embase d'ancrage osseux peut être en alliage de titane, de vanadium et d'aluminium connu sous la référence TA6V. The present invention also aims to overcome this significant disadvantage. The implant concerned. According to the invention, the element comprising said conical cavity has at least one groove formed in its wall delimiting the periphery of this conical cavity, this groove opening into this cavity. The inventor has in fact discovered that such a groove makes it possible to increase by approximately 20% the tensile strength of the assembly of the articular part to the bone anchoring base, and to increase by approximately 30%. % the torsional strength of the same assembly, thereby obtaining a fully sufficient assembly strength to withstand the repeated forces exerted on the scapula implant by certain movements of the person fitted. The respective slopes of said conical cavity and said male conical portion could be identical; preferably, however, they are different from each other, from 3 to 10 minutes of angle, which, in combination with said groove, provides a perfectly resistant assembly of the articular part to the base bone anchor. This difference in slope is preferably 5 minutes of angle, and, according to one embodiment of the invention in this case, the slope of said conical cavity is 5 ° 45 'and that of said male conical portion is 5 ° 40 '. The elements may be of any suitable implantable material. In particular, the joint piece can be made of chromium and cobalt alloy and the bone anchoring base can be made of titanium, vanadium and aluminum alloy known under the reference TA6V.

Avantageusement, l'élément ne comprenant pas la cavité conique présente un ergot apte à être engagé de manière ajustée dans ladite rainure et à coulisser dans celle-ci lors de l'assemblage des deux éléments l'un à l'autre. Cette rainure et cet ergot forment ainsi des moyens de positionnement angulaire d'un élément par rapport à l'autre, permettant d'assurer une orientation angulaire déterminée de la pièce articulaire par rapport à l'embase d'ancrage osseux. De préférence, ladite rainure et ledit ergot sont aménagés radialement sur les éléments respectifs. Selon une forme de réalisation possible de l'invention, ladite rainure est aménagée sur la pièce articulaire et ledit ergot est aménagé sur l'embase d'ancrage 35 osseux. Advantageously, the element not comprising the conical cavity has a lug adapted to be fitly engaged in said groove and to slide therein during the assembly of the two elements to one another. This groove and this lug thus form means for angular positioning of one element relative to the other, making it possible to ensure a determined angular orientation of the articular part relative to the bone anchoring base. Preferably, said groove and said lug are arranged radially on the respective elements. According to a possible embodiment of the invention, said groove is arranged on the articular part and said lug is arranged on the bone anchoring base.

L'ergot forme ainsi un moyen de repérage de la position angulaire d'implantation de l'embase d'ancrage osseux sur l'omoplate, et donc de repérage de la position angulaire qu'aura la pièce articulaire après mise en place sur cette embase d'ancrage osseux. The lug thus forms a means of locating the angular position of implantation of the bone anchoring base on the shoulder blade, and thus locating the angular position that the joint piece will have after being placed on this base. bone anchor.

Un élément pourrait comprendre plusieurs rainures et l'autre élément pourrait comprendre plusieurs ergots correspondants. Selon une forme de réalisation préférée de l'invention, toutefois, l'un desdits éléments comprend une unique rainure telle que précitée et l'autre élément comprend un unique ergot tel que précité. L'invention sera bien comprise, et d'autres caractéristiques et avantages de celle-ci apparaîtront, en référence au dessin schématique annexé, représentant, à titre d'exemple non limitatif, une forme de réalisation préférée d'un implant d'omoplate qu'elle concerne. La figure 1 est une vue en perspective, montrant, sur la droite de la figure, une embase d'ancrage à l'omoplate selon un premier angle de vue, et, sur la gauche de la figure, une pièce articulaire destinée à être montée sur cette embase d'ancrage, cette pièce articulaire étant vue selon un deuxième angle, sensiblement perpendiculaire audit premier angle de vue ; la figure 2 est une vue en perspective de la pièce articulaire, similaire à la figure 1 mais après un pivotement de cette pièce articulaire selon son axe, sur un 20 angle de 90° ; la figure 3 est une vue de l'embase d'ancrage par sa face proximale, selon l'axe de cette embase ; la figure 4 est une vue de l'embase d'ancrage et de la pièce articulaire en coupe passant par leurs axes, avant l'assemblage de la pièce articulaire à l'embase 25 d'ancrage ; et la figure 5 est une vue de l'embase d'ancrage et de la pièce articulaire similaire à la figure 4, après l'assemblage de la pièce articulaire à l'embase d'ancrage. La figure 1 représente un implant d'omoplate 1 faisant partie d'une prothèse d'articulation de l'épaule, comprenant une embase 2 d'ancrage à l'omoplate et une 30 pièce articulaire 3 formant une surface articulaire 4. Cette surface articulaire 4 est destinée à coopérer avec une surface articulaire complémentaire que forme une tige médullaire (non représentée) destinée à être insérée dans le canal médullaire de l'humérus. L'embase 2 présente une tête 5 et une queue d'ancrage 6. One element could have a plurality of grooves and the other element could have a plurality of corresponding lugs. According to a preferred embodiment of the invention, however, one of said elements comprises a single groove as mentioned above and the other element comprises a single lug as mentioned above. The invention will be better understood, and other features and advantages thereof will become apparent, with reference to the attached schematic drawing, showing, by way of non-limiting example, a preferred embodiment of a scapula implant that 'it relates to. FIG. 1 is a perspective view showing, on the right of the figure, an anchoring base on the scapula at a first angle of view, and on the left of the figure, a joint piece intended to be mounted. on this anchoring base, this articular part being seen at a second angle substantially perpendicular to said first viewing angle; Figure 2 is a perspective view of the joint piece, similar to Figure 1 but after a pivoting of this articular part along its axis, at a 90 ° angle; Figure 3 is a view of the anchor base by its proximal face, along the axis of this base; Figure 4 is a view of the anchoring base and the articular part in section passing through their axes, before the assembly of the articular part to the base 25 anchoring; and Figure 5 is a view of the anchor base and the joint part similar to Figure 4, after the assembly of the joint part to the anchor base. FIG. 1 shows a scapula 1 implant forming part of a shoulder joint prosthesis, comprising a base 2 for anchoring to the scapula and an articular part 3 forming an articular surface 4. This articular surface 4 is intended to cooperate with a complementary articular surface that forms a medullary stem (not shown) intended to be inserted into the medullary canal of the humerus. The base 2 has a head 5 and an anchor tail 6.

La tête 5 forme sur sa périphérie une surface conique 7 ayant une pente de 5°40', et constitue ainsi une partie conique mâle d'assemblage à la pièce articulaire 3. Au niveau de sa face proximale, elle présente une cavité 8 à fond courbe, dans le centre de laquelle débouche un trou 9 aménagé dans la queue d'ancrage 6. Ce trou 9 est destiné à recevoir une tige de centrage 15 que comprend la pièce articulaire 3 ; en référence aux figures 3 et 4, il apparaît qu'il présente une portion cylindrique proximale et une portion hexagonale distale, de plus faible section débouchant dans le fond de cette portion cylindrique. Cette portion hexagonale distale est destinée à recevoir de manière ajustée une portion hexagonale correspondante d'un instrument de pose de l'embase 2, permettant de réaliser une orientation angulaire de cette embase 2 sur l'omoplate. L'embase 2 comprend également quatre trous 10a, 10b aménagés autour de ce trou central 8, destinés à recevoir des vis complémentaires d'ancrage (non représentées), et un ergot 11 faisant saillie radialement du bord proximal de la tête 5. The head 5 forms on its periphery a conical surface 7 having a slope of 5 ° 40 ', and thus constitutes a male conical portion of assembly to the joint piece 3. At its proximal face, it has a cavity 8 at the bottom curve, in the center of which opens a hole 9 arranged in the anchoring tail 6. This hole 9 is intended to receive a centering rod 15 that comprises the articular part 3; with reference to Figures 3 and 4, it appears that it has a proximal cylindrical portion and a distal hexagonal portion of smaller section opening into the bottom of this cylindrical portion. This distal hexagonal portion is adapted to fitly receive a corresponding hexagonal portion of an instrument for installing the base 2, to perform an angular orientation of this base 2 on the shoulder blade. The base 2 also comprises four holes 10a, 10b arranged around this central hole 8, intended to receive additional anchoring screws (not shown), and a lug 11 projecting radially from the proximal edge of the head 5.

Comme le montre la figure 3, une première paire de trous 10a est aménagée dans le même plan diamétral que celui dans lequel s'étend l'ergot 11, et une deuxième paire de trous 10b est aménagée dans un plan diamétral perpendiculaire à ce plan. Les axes des deux trous 10a, 10b d'une même paire divergent par rapport à l'axe de la queue 6, compte tenu de la courbure que forme le fond de la cavité 8. As shown in Figure 3, a first pair of holes 10a is arranged in the same diametral plane as that in which the lug 11 extends, and a second pair of holes 10b is arranged in a diametral plane perpendicular to this plane. The axes of the two holes 10a, 10b of the same pair diverge with respect to the axis of the shank 6, taking into account the curvature formed by the bottom of the cavity 8.

Comme cela est visible sur la figure 3, chaque trou 10a, 10b présente, sur un secteur de sa circonférence, des rainures aménagée dans l'embase 2, et n'en présente pas sur le secteur diamétralement opposé ; les secteurs des trous 10a comprenant ces rainures sont tournés vers le trou 9 tandis que les secteurs des trous 10b comprenant ces rainures sont tournés du côté opposé au trou 9. Les vis destinées à être engagées dans ces trous 10a, 10b présentent des têtes coniques filetées ; les rainures d'un trou permettent une interruption du filetage de ce trou, ce qui autorise un engagement d'une vis dans ce trou avec inclinaison vers le côté du trou sur lequel se trouve le secteur dépourvu de rainures. L'embase 2 permet ainsi que les vis engagées respectivement dans le trou 10a supérieur dans le trou 10a inférieur puissent être orientées de façon optimale pour un ancrage respectivement dans le pilier de la coracoïde et dans le pilier de l'omoplate, en interdisant par conséquent une orientation de ces vis risquant de venir en conflit avec la queue d'ancrage 6 ou avec la zone osseuse dans laquelle cette queue 6 est implantée ; cette embase 2 permet également que les vis engagées dans les trous 10b soient implantées dans la partie épaisse desdits piliers en interdisant une orientation de ces vis risquant de les faire déboucher en dehors de ces piliers. Ce système formé par des trous comprenant des secteurs à encoches et des secteurs opposés dépourvus d'encoches, et par des vis à têtes coniques filetées, a fait l'objet de la demande de brevet français N° 11 54791, au nom de la demanderesse, à laquelle il sera possible de se référer pour de plus amples détails. La queue d'ancrage 6 présente quant à elle des saillies circulaires externes de prise d'appui dans l'os de l'omoplate et une cavité filetée distale 13 permettant la mise en place éventuelle d'une pièce de prolongation, pour le cas où un ancrage osseux plus profond de l'embase 2 serait requis. La pièce articulaire 3 présente, outre la surface articulaire 4 et la tige 15, une cavité 16 de forme conique, une rainure radiale 17, une cavité de fond 18 et deux logements 19. La cavité 16 débouche dans la face de la pièce articulaire 3 destinée à être tournée vers l'os. Elle a une pente de 5°45' et est destinée à recevoir la tête 5 avec coincement afin de réaliser l'assemblage de la pièce articulaire 3 à l'embase 2. Comme cela est visible sur les figures 1 et 2, cette cavité 16 est décentrée par rapport à l'axe de l'ensemble de la pièce articulaire 3, permettant ainsi de décentrer la surface articulaire 4 par rapport à l'axe de l'embase 2. Ce décentrement permet de prévenir le problème connu pour les prothèses d'épaule dit « phénomène d'encoche ». La rainure 17 est aménagée dans la paroi de la pièce articulaire 3 délimitant la périphérie de la cavité 16 et débouche dans cette cavité. Elle est apte à recevoir l'ergot 11 de manière ajustée mais avec possibilité de coulissement de cet ergot 11 en elle lors de cet assemblage. La cavité de fond 18 permet de réduire la quantité de matière constituant la pièce articulaire 3. Les logements 19 sont aménagés de manière diamétralement opposée ; ils permettent la préhension de la pièce articulaire 3 par un instrument permettant la manipulation de cette pièce articulaire et son impaction sur la tête 5. Dans l'exemple représenté, ils sont aménagés selon un plan perpendiculaire à celui dans lequel s'étend la rainure 17 En pratique, l'embase 2 est mise en place sur l'omoplate avec possibilité de repérage de la position angulaire de cette embase par rapport à l'omoplate, grâce à l'ergot 11. Une ou plusieurs vis sont ensuite mises en place dans un ou plusieurs des trous 10a, 10b afin de sécuriser l'ancrage à l'os de cette embase 2. La pièce articulaire 3 est ensuite assemblée à l'embase 2 par engagement de sa paroi délimitant la périphérie de sa cavité 16 sur la paroi 7 de la tête 5. Au cours de cet engagement, la rainure 17 et l'ergot 11 forment conjointement des moyens de positionnement angulaire de la pièce articulaire 3 par rapport à l'embase 2, permettant d'assurer une orientation angulaire adéquate de cette pièce articulaire par rapport à cette embase. Une fois l'assemblage réalisé, il apparaît que la résistance de cet assemblage à la traction est de l'ordre de 20 % supérieur à la résistance à la traction qu'a l'assemblage d'une pièce articulaire dépourvue de rainure 17 à une embase 2 ; la résistance à la torsion de cet assemblage est par ailleurs de l'ordre de 30 0/0 supérieur à la résistance à la torsion qu'a l'assemblage d'une pièce articulaire dépourvue de rainure 17 à une embase 2, comme l'illustrent les résultats détaillés ci- après. Lors d'essais confidentiels, les charges de désassemblage suivantes ont été mesurées sur cinq implants 1 conformes à l'invention, lors d'essais en traction statique (force de mise en place de 2kN ; vitesse de traction : 0,48 mm/min) : 1432 Newtons, 1450 Newtons, 1328 Newtons, 1320 Newtons et 1261 Newtons, soit une moyenne de 1358 Newtons ; les charges de désassemblage suivantes ont été mesurées sur cinq implants dont les pièce articulaires sont dépourvues de rainures telles que précitées, dans les mêmes conditions d'essais : 1141 Newtons, 1115 Newtons, 1096 Newtons, 1180 Newtons et 1081 Newtons, soit une moyenne de 1123 Newtons. As can be seen in FIG. 3, each hole 10a, 10b has, on a sector of its circumference, grooves formed in the base 2, and does not have any on the diametrically opposed sector; the sectors of the holes 10a comprising these grooves are turned towards the hole 9 while the sectors of the holes 10b comprising these grooves are turned on the opposite side to the hole 9. The screws intended to be engaged in these holes 10a, 10b have threaded conical heads ; the grooves of a hole allow an interruption of the threading of this hole, which allows a commitment of a screw in this hole with inclination towards the side of the hole on which is the sector devoid of grooves. The base 2 thus allows the screws engaged respectively in the upper hole 10a in the lower hole 10a can be optimally oriented for an anchoring respectively in the pillar of the coracoid and in the abutment of the scapula, thereby prohibiting an orientation of these screws may conflict with the anchor tail 6 or with the bone area in which the tail 6 is implanted; this base 2 also allows the screws engaged in the holes 10b are located in the thick part of said pillars by prohibiting an orientation of these screws may cause them to open out of these pillars. This system formed by holes comprising notched sectors and opposite sectors devoid of notches, and screws with conical threaded heads, was the subject of the French patent application No. 11 54791, in the name of the applicant , to which it will be possible to refer for further details. The anchoring tail 6 has for its part external circular projections of support in the bone of the scapula and a distal threaded cavity 13 for the possible establishment of an extension piece, for the case where a deeper bone anchorage of the base 2 would be required. The articular part 3 has, in addition to the articular surface 4 and the rod 15, a conically shaped cavity 16, a radial groove 17, a bottom cavity 18 and two housings 19. The cavity 16 opens into the face of the articular part 3 intended to be turned to the bone. It has a slope of 5 ° 45 'and is intended to receive the head 5 with jamming to achieve the assembly of the articular part 3 to the base 2. As can be seen in Figures 1 and 2, this cavity 16 is off-center with respect to the axis of the assembly of the articular part 3, thus making it possible to off-center the articular surface 4 with respect to the axis of the base 2. This decentering makes it possible to prevent the known problem for prostheses shoulder says "notch phenomenon". The groove 17 is arranged in the wall of the articular part 3 defining the periphery of the cavity 16 and opens into this cavity. It is adapted to receive the lug 11 in a controlled manner but with the possibility of sliding of this lug 11 in it during this assembly. The bottom cavity 18 reduces the amount of material constituting the joint part 3. The housing 19 are arranged diametrically opposite; they allow the gripping of the articular part 3 by an instrument allowing the manipulation of this articular piece and its impaction on the head 5. In the example shown, they are arranged in a plane perpendicular to that in which the groove 17 extends. In practice, the base 2 is placed on the shoulder blade with the possibility of locating the angular position of this base relative to the scapula, thanks to the lug 11. One or more screws are then placed in place. one or more of the holes 10a, 10b to secure the anchoring to the bone of this base 2. The articular part 3 is then assembled to the base 2 by engagement of its wall delimiting the periphery of its cavity 16 on the wall 7 of the head 5. During this engagement, the groove 17 and the lug 11 together form means for angular positioning of the articular part 3 relative to the base 2, to ensure adequate angular orientation of this articular part relative to this base. Once assembled, it appears that the resistance of this assembly to traction is of the order of 20% greater than the tensile strength of the assembly of a joint piece devoid of groove 17 to a base 2; the torsional strength of this assembly is moreover of the order of 30% greater than the torsional strength of the assembly of an articular part devoid of a groove 17 to a base 2, such as the illustrate the results detailed below. In confidential tests, the following disassembly loads were measured on five implants 1 according to the invention, during static tensile tests (2kN positioning force, tensile speed: 0.48 mm / min ): 1432 Newtons, 1450 Newtons, 1328 Newtons, 1320 Newtons, and 1261 Newtons, an average of 1358 Newtons; the following disassembly loads were measured on five implants whose articular parts are devoid of grooves as above, under the same test conditions: 1141 Newtons, 1115 Newtons, 1096 Newtons, 1180 Newtons and 1081 Newtons, an average of 1123 Newtons.

S'agissant de la résistance à la torsion, les couples maximaux suivants ont été mesurés sur cinq implants 1 conformes à l'invention (force de mise en place de 2kN ; vitesse de torsion : 20°/min) : 40,4 N.m, 32,5 N.m, 46,0 N.m, 33,5 N.m 34,6 N.m soit une moyenne de 37,4 N.m ; les couples maximaux suivants ont été mesurés sur cinq implants dont les pièce articulaires sont dépourvues de rainures telles que précitées, dans les mêmes conditions d'essais : 28,5 N.m, 31,5 N.m, 29,4 N.m, 27,8 N.m 27,4 N.m soit une moyenne de 28,9 N.m. L'invention fournit par conséquent un implant d'omoplate 1, ou tout autre type d'implant à embase d'ancrage osseux et pièce articulaire formant une surface articulaire, ayant pour avantages déterminants de : - permettre d'obtenir une résistance d'assemblage pleinement suffisante pour supporter les efforts répétés exercés sur l'implant 1 par certains mouvements de la personne appareillée ; - comprendre des moyens 11, 17 de positionnement angulaire d'un élément 2, 3 par rapport à l'autre, à même d'assurer une orientation angulaire déterminée de la pièce articulaire 3 par rapport à l'embase 2, l'ergot 11 formant en outre un moyen de repérage de la position angulaire d'implantation de l'embase 2 sur l'omoplate. L'invention a été décrite ci-dessus en référence à une forme de réalisation fournie à titre d'exemple. Il va de soi qu'elle n'est pas limitée à cette forme de réalisation mais qu'elle s'étend à toutes les autres formes de réalisation couvertes par les revendications ci-annexées. With regard to the torsion resistance, the following maximum torques were measured on five implants 1 according to the invention (delivery force of 2kN, torsion speed: 20 ° / min): 40.4 Nm, 32.5 Nm, 46.0 Nm, 33.5 Nm 34.6 Nm, an average of 37.4 Nm; the following maximum torques were measured on five implants whose articular parts are devoid of grooves as mentioned above, under the same test conditions: 28.5 Nm, 31.5 Nm, 29.4 Nm, 27.8 Nm 27 , 4 Nm is an average of 28.9 Nm The invention therefore provides a scapula 1 implant, or any other type of implant with a bone anchoring base and articular piece forming a joint surface, having the following key advantages: - to obtain an assembly resistance fully sufficient to withstand the repeated forces exerted on the implant 1 by certain movements of the fitted person; - Including means 11, 17 of angular positioning of an element 2, 3 relative to the other, able to ensure a specific angular orientation of the articular part 3 relative to the base 2, the lug 11 further forming means for locating the angular position of implantation of the base 2 on the scapula. The invention has been described above with reference to an embodiment provided by way of example. It goes without saying that it is not limited to this embodiment but that it extends to all other embodiments covered by the appended claims.

Claims (9)

REVENDICATIONS1 - Implant (1) faisant partie d'une prothèse d'articulation, notamment implant (1) d'omoplate faisant partie d'une prothèse d'articulation de l'épaule, comprenant une embase (2) d'ancrage osseux et une pièce articulaire (3) formant une surface articulaire (4), l'un de ces deux éléments (3) comprenant une cavité conique (16) à faible pente tandis que l'autre élément (2) comprend une partie conique mâle (5) correspondante, cette partie conique mâle (5) étant destinée à être insérée dans ladite cavité conique (16) jusqu'à complet coincement dans celle-ci ; caractérisé en ce que l'élément (3) comprenant ladite cavité conique (16) présente au moins une rainure (17) aménagée dans sa paroi délimitant la périphérie de cette cavité conique (16), cette rainure (17) débouchant dans cette cavité. CLAIMS1 - Implant (1) forming part of a joint prosthesis, in particular implant (1) of scapula forming part of a shoulder joint prosthesis, comprising a base (2) for bone anchoring and a articular piece (3) forming an articular surface (4), one of these two elements (3) comprising a conical cavity (16) with a slight slope while the other element (2) comprises a male conical part (5) corresponding, this male conical portion (5) being adapted to be inserted into said conical cavity (16) until complete wedging therein; characterized in that the element (3) comprising said conical cavity (16) has at least one groove (17) formed in its wall defining the periphery of the conical cavity (16), the groove (17) opening into this cavity. 2 - Implant (1) selon la revendication 1, caractérisé en ce que les pentes respectives de ladite cavité conique (16) et de ladite partie conique mâle (5) sont différentes l'une de l'autre, de 3 à 10 minutes d'angle 2 - Implant (1) according to claim 1, characterized in that the respective slopes of said conical cavity (16) and said male conical portion (5) are different from each other, from 3 to 10 minutes d 'angle 3 - Implant (1) selon la revendication 2, caractérisé en ce que ladite différence de pente est de 5 minutes d'angle. 3 - Implant (1) according to claim 2, characterized in that said difference in slope is 5 minutes of angle. 4 - Implant (1) selon la revendication 3, caractérisé en ce que la pente de ladite cavité conique (16) est de 5°45' et en ce que la pente de ladite partie conique mâle (5) est de 5°40'. 4 - Implant (1) according to claim 3, characterized in that the slope of said conical cavity (16) is 5 ° 45 'and in that the slope of said male conical portion (5) is 5 ° 40' . 5 - Implant (1) selon l'une des revendications 1 à 4, caractérisé en ce que la pièce articulaire (3) est en alliage de chrome et de cobalt et en ce que l'embase (2) d'ancrage osseux est en alliage de titane, de vanadium et d'aluminium connu sous la référence TA6V. 5 - Implant (1) according to one of claims 1 to 4, characterized in that the joint piece (3) is chromium alloy and cobalt and in that the base (2) of bone anchoring is in titanium, vanadium and aluminum alloy known as TA6V. 6 - Implant (1) selon l'une des revendications 1 à 5, caractérisé en ce que l'élément (2) ne comprenant pas la cavité conique (16) présente un ergot (11) apte à être engagé de manière ajustée dans ladite rainure (17) et à coulisser dans celle-ci lors de l'assemblage des deux éléments (2, 3) l'un à l'autre. 6 - Implant (1) according to one of claims 1 to 5, characterized in that the element (2) not comprising the conical cavity (16) has a lug (11) adapted to be engaged in a manner adjusted in said groove (17) and to slide therein during the assembly of the two elements (2, 3) to one another. 7 - Implant (1) selon la revendication 6, caractérisé e n ce q ue ladite rainure (17) et ledit ergot (11) sont aménagés radialement sur les éléments (2, 3) respectifs. 7 - Implant (1) according to claim 6, characterized in that q said groove (17) and said lug (11) are arranged radially on the elements (2, 3) respectively. 8 - Implant (1) selon la revendication 5 ou la revendication 6, caractérisé en ce que ladite rainure (17) est aménagée sur la pièce articulaire (3) et ledit ergot (11) est aménagé sur l'embase (2) d'ancrage osseux. 8 - Implant (1) according to claim 5 or claim 6, characterized in that said groove (17) is arranged on the articular part (3) and said lug (11) is arranged on the base (2) of bone anchorage. 9 - Implant (1) selon l'une des revendications 6 à 8, caractérisé en ce que l'un desdits éléments (3) comprend une unique rainure (17) telle que précitée et en ce que l'autre élément (2) comprend un unique ergot (11) tel que précité. 9 - Implant (1) according to one of claims 6 to 8, characterized in that one of said elements (3) comprises a single groove (17) as mentioned above and in that the other element (2) comprises a single lug (11) as mentioned above.
FR1156282A 2011-07-11 2011-07-11 IMPLANT FORMING PART OF A PROSTHESIS OF ARTICULATION, PARTICULARLY IMPLANT OF OMOPLATE FORMING PART OF A PROSTHESIS OF ARTICULATION OF THE SHOULDER Active FR2977791B1 (en)

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EP3090705A1 (en) * 2015-05-05 2016-11-09 Tornier, Inc. Glenoid implant
EP3649987A1 (en) * 2015-03-19 2020-05-13 Limacorporate SPA Improved glenoid anchor for a shoulder joint prosthesis
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FR2955247B1 (en) 2010-01-21 2013-04-26 Tornier Sa GLENOIDAL COMPONENT OF SHOULDER PROSTHESIS
FR2971144A1 (en) 2011-02-08 2012-08-10 Tornier Sa GLENOIDAL IMPLANT FOR SHOULDER PROSTHESIS AND SURGICAL KIT
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EP3697347A2 (en) 2017-10-16 2020-08-26 Imascap SAS Shoulder implants
JP7478810B2 (en) 2019-08-09 2024-05-07 ハウメディカ オステオニクス コーポレイション Shoulder surgery kit

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WO2016147163A1 (en) * 2015-03-19 2016-09-22 Limacorporate S.P.A. Improved glenoid anchor for a shoulder joint prosthesis
EP3649987A1 (en) * 2015-03-19 2020-05-13 Limacorporate SPA Improved glenoid anchor for a shoulder joint prosthesis
EP3936086A1 (en) * 2015-03-19 2022-01-12 Limacorporate S.p.A. Improved glenoid anchor for a shoulder joint prosthesis
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EP3090705A1 (en) * 2015-05-05 2016-11-09 Tornier, Inc. Glenoid implant
EP3679899A1 (en) * 2015-05-05 2020-07-15 Tornier, Inc. Glenoid implant
GB2616360A (en) * 2019-03-12 2023-09-06 Arthrosurface Inc Humeral and glenoid articular surface implant systems and methods
GB2616360B (en) * 2019-03-12 2023-11-29 Arthrosurface Inc Humeral and glenoid articular surface implant systems and methods

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