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.

An apparatus and methods are provided for a tapered implant for treating osteochondral/subchondral defects. The tapered implant comprises a top portion that includes a shape that approximates an osteochondral/subchondral surface to be replaced. A bottom portion of the tapered implant is configured to be implanted into a hole drilled in bone. A cylindrical sidewall of the tapered implant has a diameter that generally decreases from a first diameter of the top portion to a second diameter of the bottom portion. The tapered implant comprises any homogenous synthetic or natural material suitable for implantation into bone, including any of collagen, human or animal allograft, silicone, bioglass, peek, polyethylene, titanium, and cobalt chrome, and any combination thereof.

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.

An orthopaedic implant includes an implant body having a first surface and a second surface opposite the first surface. The second surface includes a fixation feature. The fixation feature is configured to have a variable width for fastening the implant to a fixation bore formed in a bone. The implant body is D-shaped and has a straight edge and a curved edge. A length of the fixation feature is substantially parallel to the straight edge of the implant body. The fixation feature is configured to have a width that tapers along the length of the fixation feature.

A subtalar implant for arthroereisis of the talocalcaneal joint. The implant is intended to be inserted into the talocalcaneal joint via its lateral orifice and has an oblong shape that extends longitudinally along an axis of insertion of the implant. The implant includes: a head with the shape of a cone of revolution centred on the axis of insertion; an anchoring thread; and a rod having the shape of a cylinder of revolution. The rod has, on its surface, the anchoring thread and being configured to be inserted up to the axis of rotation of the talocalcaneal joint. The head has, on its radially outer surface, a retaining element for retaining the implant in rotation about the axis of insertion, the retaining element exerting retention against a colonising tissue.

An orthopedic implant comprises a body having an articulating surface and a surface opposite the articulating surface. The surface opposite the articulating surface includes a fixation feature. The fixation feature is configured to have a variable width for fastening the implant to a fixation bore formed in a bone.

A bent trial femoral neck (400) and method for visually assessing the orientation of an acetabular cup implanted in a pelvis of a patient are described. The bent trial femoral neck comprises a body (402) extending along a femoral neck axis, an attachment formation (408, 410) extending from the body for releasably attaching the trial femoral neck to a femoral part received with a femur of the patient and a taper (404). The taper extends along a taper axis and the taper axis is tilted anteriorly relative to the femoral neck axis by an angle configured to position a trial femoral head having an indicium on an outer surface so that the indicium is parallel to a plane of a rim of the acetabular cup, or a rim of a liner within the acetabular cup, when the acetabular cup is oriented in the pelvis of the patient with a target orientation and the hip joint is in a predetermined position.

The present disclosure relates to a system for augmentation of a tibial component. The system includes an augmentation component having a first porous structure, a second porous structure, a top portion having a top surface, and a bottom portion having a bottom surface arranged opposite the augmentation component from the top surface. The system also includes a tibial component and an instrument, with the tibial component being configured to couple to the augmentation component. The instrument includes an engagement portion having a geometry complimentary to that of the augmentation component. Further, a method of augmenting a tibial component is disclosed with the steps of collecting imaging data from a patient, identifying a void in the distal tibia, obtaining an augmentation component that corresponds to the void, coupling the augmentation component to the tibial component and implanting the tibial component into the tibia so the augmentation component occupies the tibial void.

A subtalar implant for arthroereisis of the talocalcaneal joint. The implant being intended to be inserted into the talocalcaneal joint via its lateral orifice and having an oblong shape that extends longitudinally along an axis of insertion of the implant. The implant includes: a head with the shape of a cone of revolution centred on the axis of insertion; an anchoring thread; and a rod having the shape of a cylinder of revolution. The rod has, on its surface, the anchoring thread and being intended to be inserted up to the axis of rotation of the talocalcaneal joint. The head has, on its radially outer surface, a retaining element for retaining the implant in rotation about the axis of insertion, the retaining element being exerting retention against a colonising tissue.

An orthopedic implant comprises a body having an articulating surface and a surface opposite the articulating surface. The surface opposite the articulating surface includes a fixation feature. The fixation feature is configured to have a variable width for fastening the implant to a fixation bore formed in a bone.