419 results about "Humerus" patented technology

A method for implanting an intra-articular shoulder prosthesis is provided. The method includes removing a proximal portion of a humerus. The proximal portion of the humerus preferably forms a resected portion. The resected portion has a convex outer surface and an inner surface. The method further includes engaging the convex outer surface of the resected portion with a cut surface of the proximal portion of the humerus. The cut surface of the proximal portion of the humerus and/or the inner surface of the resected portion are optionally processed to form a generally concave surface, such as by impacting. In one embodiment, the inner surface of the resected portion is impacted into engagement with the cut surface of the proximal portion of the humerus. The generally concave inner surface of the resected portion forms a concave articular surface to receive an interpositional implant.

A method of performing a shoulder joint surgery involving a scapula having a glenoid cavity, a humerus and a humeral ball on a surgical table includes mounting a retractor support to the surgical table and positioning the retractor support about the shoulder joint. The skin and flesh layers proximate the shoulder joint are incised and the skin and flesh layers are manually retracted with a retractor. The retractor is secured in a selected position by attaching the retractor to the retractor support.

An implant assembly and associated method for selectively performing reverse and traditional arthroplasty for a shoulder joint that includes a humerus and a glenoid. The implant assembly may include a head, a cup, a humeral stem and an adaptor. The method includes inserting the humeral stem to the humerus and connecting a male taper of the adaptor to a female taper of the head. For reverse arthroplasty, the method includes attaching the adaptor to the glenoid and the cup to the stem. For traditional arthroplasty, the method includes attaching the adaptor to the humeral stem and the cup to the glenoid. The method also includes articulating the head with the cup.

The invention concerns a shoulder prosthesis assembly comprising a meta-glenoid element (7) formed by a plate (13) provided with a central tubular block (14) an anchoring members in the glenoid cavity (3), and a glenoid sphere (9) designed to top the metaglenoid element and provided with an axial screw (35) screwed into said pin; the glenoid sphere has an articulated surface (11) designed to co-operate with a cup of an associated humeral prosthesis (2); said assembly comprises means (16, 45, 46; 51, 50, 49) guiding the glenoid sphere adapted to facilitate its being fixed on the meta-glenoid element; said means comprise a pin (46) adapted to be slotted into the tubular block (14) and into an axial passage of the screw (35); the glenoid sphere (9) is thus guided by being slid on the pin (46) until the screw (35) is inserted precisely into the axis of the tubular block (14), wherein it can be screwed without any risk of damaging the thread on the screw and the internal thread of the block. Advantageously, the free end (48) of the screw (35) can likewise be bevelled to facilitate its being inserted in the block (14) without damaging the threads. The inventive arrangement is particular useful considering the difficulties encountered by the surgeon for correctly positioning the glenoid sphere (9) relative to the meta-glenoid element (7) owing to lack of visibility.

A prosthetic elbow for replacing an elbow of a dog or a human to restore normal, pain-free joint function. The elbow includes a humeral component for attachment to a humerus and a radioulnar component for attachment to an ulna. The humeral component includes a generally cylindric spool having a contoured external surface defining a first articular surface. The radioulnar component has a generally U-shaped contour with an inner peripheral surface defining a second articular surface sized and shaped for engagement with the first articular surface. Positional guides provide for implantation at precise locations.

This invention relates to an elbow prosthesis comprising a humeral component forming a first, substantially cylindrical articulating surface and an ulnar component forming a second articulating surface adapted to be arranged around a part of this first articulating surface and to pivot about a longitudinal axis of this first articulating surface. The ulnar component is provided with the means for mounting a locking element forming a third articulating surface, extending the second articulating surface and adapted to be disposed around the first articulating surface, these second and third articulating surfaces extending together, in transverse section, over more than 180° about the first articulating surface.

The glenoid component according to the invention comprises a metal body of which the inner face is adapted to be immobilized on the glenoid cavity of a shoulder and of which the outer face bears a concave articulating surface adapted to cooperate with a humeral component. This articulating surface extends on the periphery by a convex surface forming, at least in part, the edge of the body.

A two piece humeral component for use in joint arthroplasty which is adapted to be implanted into a joint and engaged by a socket component of the joint. The joint component includes a body having a first articulating surface and a second medial surface opposite the first articulating surface. The first articulating surface is adapted to be engaged by the socket and the second medial surface is adapted to be secured to mounting portion. The mounting portion has a first surface and a second medial surface. The first surface is adapted to be fixably engaged to the second mounting portion of the humeral component. The second medial surface is adapted to be secured to the humerus. A peg which has a first end adapted to engage a cavity found in the humerus is disposed on the mounting portion's second medial surface.

In a first aspect the present invention provides a glenoid prosthesis assembly for use in shoulder joint arthroplasty to address conditions where deterioration of the rotator cuff mechanism of the shoulder joint is severe, the assembly comprising a first shell component to be affixed to a scapula by fixing means, and a smaller second component adapted to nest within the first component and having an articulation surface for articulating with a humeral head, the first component being over-sized relative to the glenoid surface of a scapula whereby the first component may be first affixed to at least two of the glenoid, acromion and coracoid processes of the scapula in use by the fixing means and the second component may be cemented in place within the first component allowing initial adjustability in the poise of the second component relative to the first component. Amongst other aspects the invention also provides a modular proximal humeral prosthesis system for use in shoulder joint arthroplasty which enables the proximal humeral prosthesis to be changed between anatomical and reverse of anatomical configurations to address differing degrees of shoulder joint deterioration.

A total elbow arthroplasty system, incorporating a humeral component, a radial component and a ball component, may be used as a total elbow replacement in the canine, as well as in other species. The implant of the present invention has an isometric humeral component and an isometric radial component. An isometric ball component having an isometric articular surface is mounted on the radial component. The humeral and radial components have stems for mounting in the medullary canals of the respective bones, which are angled so as to approximate the configuration of the original humerus and radius. The components work together to form a nonconstrained ball and socket joint. The invention is also directed to methods for implanting the novel endoprosthesis of the present invention in a canine elbow joint. The apparatus and methods of the present invention are useful in the treatment of elbow osteoarthritis in canines, as well as in other species, including other quadrupeds and humans.

Inverse prosthesis of the shoulder for the articulation of a humerus in a scapula of a shoulder comprising a glenoid cavity. The prosthesis includes an at least partly convex articulation element, including elements for support and attachment to the glenoid cavity, and able to articulate with an at least partly concave mating articulation element, associated with the top of the humerus. The articulation element includes a substantially hemi-spherical element and a pin-type implant element made as distinct and reciprocally removable elements, so as to allow them to be assembled sequentially with respect to the glenoid cavity.

A bone plate for fixation of proximal humerus fractures comprises an elongated shaft portion having a first width and a head portion connected to the shaft portion having a second width greater than the first width. The head portion and the shaft portion define a common longitudinal axis. At least one first screw hole may be located in the head portion, and at least one second screw hole may be located in the shaft portion. At least one of the first and second holes is configured to engage a head of a bone screw to form an angularly stable connection with the bone screw.

The prosthesis of this invention comprises a humeral or femoral component presenting a concave articulation surface, and an intermediate component presenting first and second convex articulation surfaces intended to cooperate respectively with said concave articulation surface of the humeral or femoral component and with a concave glenoid or cotyloid articulation surface. The locus of the instantaneous centers of rotation of the first convex articulation surface, with respect to the concave humeral or femoral articulation surface, and the locus of the instantaneous centers of rotation of the second convex articulation surface on the glenoid or cotyloid surface, are located on either side of the first surface.

A glenoid component (100) for use with a prosthetic humeral component (102) for use in performing shoulder arthroplasty is provided. The glenoid component (100) may be fitted at least partially into a cavity (104) formed in the glenoid vault (106). The glenoid component (112) includes a body (112) having a stem portion (114) for inserting at least partially into the cavity (104) formed in the glenoid vault (106). The stem portion (114) cooperates with the interior wall (116) of the cavity (104) formed in the glenoid vault (106). The body (112) has a bearing portion (120) for articulating cooperation with the prosthetic humeral component (102).

A humeral component, forming a first articulating surface, and an ulnar component forming a second articulating surface adapted to be disposed around a part of the first articulating surface and to pivot about its longitudinal axis. This ulnar component is provided with structure for mounting a locking element which forms a third articulating surface extending the second and adapted likewise to be disposed around a part of the first surface. These mounting structure comprise guiding structures adapted to cooperate with complementary structure provided on the locking element in order to guide this element in translation with respect to the ulnar component, up to a position where blocking structure provided respectively on the locking element and on the ulnar component may be employed to immobilize this element on this component, these blocking structure being able to be employed only in this position.

Surgical procedures, tools and implants are disclosed for both conventional and reverse shoulder implant surgeries. The improved procedures, tools and implants relate to humeral head resurfacing, humeral head resection for standard implants, humeral head resection for reverse shoulder implants, glenoid resurfacing for standard shoulder implants and glenoid resurfacing for reverse shoulder implants. 3D scans and x-rays are used to develop virtual models of the patient anatomy, identify patient specific landmarks for anchoring guide wire installation blocks, templates and drill guides. 3D scans are also used to design patient specific tools and implants for the shoulder implant procedures and to pre-operatively determine the appropriate inclination and retroversion angles.

This prosthesis comprises a humeral or femoral component and an intermediate component. The concave surface of articulation of the humeral or femoral component is formed by a plate connected by a neck to a part of this component adapted to be anchored in the humeral or femoral medullary cavity. The intermediate component is provided with a member for retaining the humeral or femoral component in a position where the plate is in abutment against the first convex surface of the intermediate component. The retaining member defines a non-circular passage in which the neck is adapted to be displaced as a function of the movements of the humeral or femoral component with respect to the other components of the prosthesis. The retaining member defines with the first convex surface of articulation of the intermediate component a volume for receiving a part of the plate projecting radially with respect to the neck.

A prosthetic humeral device (1) having at least two guide holes (11) located at predetermined locations thereon for the acceptance of a fastening means (29), which is preferably a screw (16) and a predeterminedly-shaped washer (6) with at least one projection (17) located on the underside. After inserting the elongated stem (14) of the prosthetic humeral device (1) into the humerus (2), a tuberosity grasping tool (19) is used to grasp a tuberosity (4) and (7). The tuberosity (4) and (7) is then positioned to an appropriate level on the prosthetic humeral device (1), a hole is drilled into the tuberosity (4) and (7), the screw (16) with washer (6) is inserted, the grasping tool (19) is removed and the screw (16) and washer (6) are tightened.

A glenoid component used for shoulder arthroplasty is adapted to be implanted into a scapula and engaged by a head of a humeral component. The glenoid component includes a body having a first articulating surface and a second medial surface opposite to the first articulating surface. The first articulating surface is adapted to engage with a humeral head. A plurality of fixed pegs each have a first end adapted to engage a cavity formed in the scapula and a second end extending from the medial surface. A central peg fixation mechanism is provided that is configured to couple an optional central fixation peg to the medial surface.

Various embodiments of the present invention relate to an apparatus and method for reverse shoulder arthroplasty (e.g., reverse total shoulder arthroplasty). In one specific example, a glenoid component used to resurface the scapula may be provided. Of note, unlike traditional total shoulder arthroplasty the glenoid component in a reverse shoulder is convex rather than concave; it acts as a physical stop to prevent the superior migration of the humeral head—a typical occurrence in patients suffering from rotator cuff tear arthropathy (CTA).

The humeral portion of a shoulder prosthesis includes a diaphyseal component configured for fixation within the humerus, a metaphyseal component, configured for removable implantation within the metaphysis of the humerus, and an engagement mechanism for removably engaging the two components. The metaphyseal component can initially include a convex articulating surface that can be replaced with a concave surface during the shoulder arthroplasty procedure or in a subsequent revision surgery. The metaphyseal component can also include a feature to facilitate removal of the component from the bone once it has been disengaged from the diaphyseal component.

A set of at least two osteosynthesis plates (2g, 2h) for implantation, anatomical reduction and internal splinting of bone fragments, in particular after fractures of the distal humerus. The two osteosynthesis plates (2g, 2h) according to the invention are provided with drilled holes (3a, 3b, 3c) which are arranged or formed so that the bone crews (12) passing through them come to rest in different directions in space, so that bone screws (12) can pass more completely than in the past through the bone space of the splinted bone (1).

A shoulder arthroplasty kit for shoulder arthroplasty is provided. The kit includes a stem for insertion into the humerus and a first member. The first member has a surface having a convex periphery adapted for articulation with the natural glenoid fossia. The convex periphery includes a first articulating surface defining a generally circular outer periphery of the first articulating surface and a second articulating surface extending from a portion of the circular outer periphery of the first articulating surface. The first member is removably cooperable with said stem. The kit also includes a second member including a portion having a concave periphery. The second member is removably cooperable with the stem. The kit further includes a third member for insertion into the natural glenoid fossia. The third member includes a portion having a convex periphery. The third member is adapted for articulation with the second member.