A hip joint prosthesis is formed of a coil spring having a middle section bounded by first and second opposite ends, with one of the two ends configured as a femoral fixing end and the other of the two ends configured as an acetabular fixing end. A central axis of the coil spring extends between the two opposite ends, providing a freely movable, flexible central coil linking the two ends.

A sinus tarsi implant for the purpose of stabilizing and restoring motion between the talus and calcaneus while allowing normal motion and alignment. In a preferred embodiment, the implant is composed of a titanium alloy that is a combination of a cylindrical portion and an axially connected conical portion. The cylindrical portion has a surface with multiple parallel grooves that are each parallel to the transverse axis of the cylinder. The grooves are uniquely shaped with a perpendicular medial side and an angled lateral side. The implant is cannulated to enable use of a guide wire that insures proper alignment during insertion.

The present invention relates to a shoulder prosthesis comprising:a metaglene element (2) or baseplate;a pin (3) projecting from said metaglene element (2);a through-hole (11) in the centre of said metaglene element (2);at least one through-hole (5) formed in a periphery of the metaglene element (2) with respect to said central through-hole (11);a glenosphere element (12) opposite said pin (3) with respect to said metaglene element (2);a central compression screw (9) housed in said through-hole (11) in the centre of said metaglene element (2) and having a head abutting onto the bottom of said hole (11); andwherein the central through-hole (11) has an opening (11A) that is threaded in a stretch to receive the end of a safety screw (18) passing through the glenosphere element (12);a connector element (13) between the metaglene element (2) and the glenosphere element (12), the metaglene element (2) providing a seat (14) for housing the connector element (13) projecting around the central through-hole (11).

A system for a unicompartmental knee replacement is described. The system can include a femoral prosthesis component, a tibial prosthesis component and a meniscal bearing. The meniscal bearing can be insertable between the femoral prosthesis component and the tibial prosthesis component. The meniscal bearing can include a first bearing surface configured to bear against the femoral prosthesis component, a second bearing surface opposed to the first bearing surface and configured to bear against the tibial prosthesis component, and a sidewall separating the first bearing surface from the second bearing surface, wherein the sidewall has a retention groove formed in a portion thereof, and wherein the meniscal bearing and the tibial prosthesis component are configured such that the retaining flange enters the retention groove on movement of the meniscal bearing relative to the tibial prosthesis component towards the medial wall.

An intervertebral implant includes a body with a first face, a second face connected to the first face, and an axis of rotation. The body defines a hollow space for connecting to an insertion device, the hollow space being accessible through an opening formed between the first and second faces. The opening is elongate and extends around the axis of rotation to facilitate pivoting of the implant relative to the insertion device about the axis of rotation to a first angular position and a second angular position. The implant further includes a first abutment surface that engages the insertion device in a form-fit manner at the first angular position, and a second abutment surface that engages the insertion device in a form-fit manner at the second angular position. The opening can also engage the insertion device to hold the implant at at least one additional angular position.

Implants, device, systems and methods for replacing an articulation surface in a joint, for example, a reverse glenoid implant with a baseplate, a central screw, a peripheral screw, a modular taper, and a post. Methods for implanting the glenoid implant are also disclosed.

An orthopaedic fixation assembly for prosthetic biologic attachment. The orthopaedic fixation assembly may include a main body with a longitudinally-extending stem having a proximal end, a distal end, and a cavity body. An anchor plug may be configured to be received within the stem cavity, and securable thereto via complementary mating surfaces. A spindle structure may be fixedly attached to the proximal end of the longitudinally-extending stem and protrude outwardly therefrom such that a portion of the structure extends externally beyond the resected cavity of the bone that may prevent rotational motion of the spindle. The spindle structure may have at least one compliant biasing member configured to apply a compressive force to the surrounding bone. A porous coating may be at the juncture between stem and spindle structure, on the spindle, and the splines and anti-rotation chocks, improving the initial stability of the implant and facilitating long-term bone ingrowth.

A glenosphere includes a body and a flange. The body includes a first body surface and a spherical second body surface, and includes an engagement feature to engage with an attachment structure attachable to a bone. The flange extends radially outward from the body and includes a first flange surface contiguous with a first body surface and a second flange surface contiguous with the second body surface. The flange has a flange length extending from a first end and a second end such that an angle defined by a first line from a center of the body to the first end and a second line from the center of the body to the second end is less than 180 degrees.

An acetabular joint prosthesis may be designed to replace an acetabular articular surface. The prosthesis can include an acetabular cup, an augment, and an augment-securing mechanism configured to secure the augment to the cup. The mechanism can be reconfigured between an unlocked configuration in which a slider is slidable along a guide feature and a locked configuration in which the slider or guide feature is in an expanded form such that the slider is fixed in place relative to the guide feature. An unlocked configuration may include the augment-securing mechanism allowing rotation between the augment and the cup, with the augment being securable to the augment in multiple rotational positions. Also, the prosthesis may be configured to facilitate actuation between the unlocked and locked configurations, including moving an instrument to the prosthesis in an access direction that is substantially perpendicular to a rim of the cup.

The invention relates to a ceramic surface arthroplasty system, which consists of a convex, hemispherical, metallic implant (1) and a hollow hemispherical metal implant (3). The implants are coated with porcelain or zirconium oxide layer on their friction surfaces to avoid the creation of metallic microparticles. The convex implant (1) has a navel (4) on the thread (6) of which a bone-piercing pre-tensioning needle (7) is screwed and is tightened with a washer (9) at the area of the major trochanter or bulge. Further, it has protruding ribs (5) immersed on the surface of the head.