An orthopedic implant manufacturing method. The method includes preparing a pre-operative surgical plan for a specific patient, the surgical plan including a three-dimensional image of a patient's joint indicating at least one resection plane, communicating the surgical plan to a surgeon of the patient, and receiving approval of the surgical plan and the resection plane by the surgeon. The method also includes providing automated osteophyte/protrusion removal control for surgeon manipulation, receiving a modified three-dimensional image of a patient's joint indicating an osteophyte/protrusion removal and a recommendation for a corresponding selected orthopedic implant from the surgeon, and requesting manufacture of the selected orthopedic implant.

Unicondylar tibia implant devices having a bone-facing, distal side that can be detailed with cement fixation features and may include any of or a plurality of grooves, pegs, fins, rails, cavities, and/or coating whereby the geometry of the implant device improves implant-to-cement or cement-to-bone fixation characteristics exceeding that of a traditional flat surface. The implant device may also include a proximal side facing away from the bone-facing, distal side and having a geometry that provides either articulation with (cartilage and meniscal substituting) or receipt of a secondary device coupleable to the implant device on the distal side of the secondary device that features an away-from-bone facing articulating feature. Additionally, the geometry of the implant device in anterior-posterior and medial-lateral directions, among other directions, provides a variety of improvements relative to currently available devices.

A knee joint endoprosthesis set for replacing a knee joint of a patient, a patient knee joint endoprosthesis set, and a knee joint endoprosthesis system. The knee joint endoprosthesis set includes a knee joint endoprosthesis with a femoral component, a tibial component, and a first meniscal component. The knee joint endoprosthesis set also includes a second meniscal component configured differently from the first meniscal component. One of the first and second meniscal components is arranged between the femoral component and the tibial component for forming the knee joint endoprosthesis.

A surgical instrument system includes a pair of side-specific orthopaedic surgical instrument assemblies. The right-limb side-specific instrument assembly is kitted so as to be devoid of left-limb side-specific instruments and vice versa.

The present disclosure pertains to ankle prostheses. In an example embodiment, the ankle prosthesis comprises an adjustable and replaceable intermediate implant that is disposed between a tibial implant and a talar implant. The intermediate implant is adjustable relative to the tibial implant and can be interlocked therewith once adjusted. Methods of using, fitting, and adjusting the device are also described. Still other embodiments are described.

An intervertebral spacer inserter includes a sleeve having a longitudinal axis, a hollow sleeve bore extending through the sleeve along the longitudinal axis, a sleeve tip end and an opening of a passage disposed in the sleeve tip end. The passage extends into the sleeve to the sleeve shaft along a passage axis that intersects the longitudinal axis at an angle less than about 90°. A sliding tip with an elongated slot is in contact with the sleeve tip end and is moveable with respect to the sleeve tip end between a first position with the opening accessible through the elongated slot and disposed adjacent a first end of the elongated slot and a second position with the opening accessible through the elongated slot and disposed adjacent a second end of the elongated slot opposite the first end.

A surgical instrument system includes a commonly-sized orthopaedic surgical instrument assembly for use in implanting a femoral component, along with a number of orthopaedic surgical instrument assemblies having varying sizes of instruments of use in implanting a tibial tray component and a patella component.

A surgical instrument system includes a pair of side-specific orthopaedic surgical instrument assemblies. The right-limb side-specific instrument assembly is kitted so as to be devoid of left-limb side-specific instruments and vice versa.

The universal tibial insert includes a keyed lock plate generally symmetrical across a median plane and a frontal plane and is selectively engageable with an asymmetrical tibial base plate in a first orientation and a second orientation approximately 180° relative to the first orientation. This allows an upwardly presented articular surface to reciprocally interface with a medial condyle and a lateral condyle of a femoral component in articulatory relation therewith when the universal tibial insert is in either of the first orientation or the second orientation.

The present disclosure relates to a knee joint augment having an anatomical shape. More specifically, the present disclosure relates to a knee joint augment that is used for artificial joint replacement to replace lost bone, wherein the augment is used in artificial knee replacement surgery to be coupled to a knee implant. The augment includes a top surface configured to be brought into contact with a distal surface of a base plate that forms the body of a tibia element and a bottom surface configured to be brought into contact with a cut surface of a tibia. The bottom surface has an area smaller than that of the top surface, and has a tapered shape that narrows from the top to the bottom. An intermediate line at which one end surface cut to be perpendicular to the top surface and an outer surface meet each other has a shape that is outwardly convex to the outside of the augment with respect to a straight line connecting a top point where the intermediate line and the top surface meet and a bottom point where the intermediate line meets the bottom surface, whereby the intermediate line has a shape corresponding to the anatomical shape of a cut bone.