A method for preparing a femur for receiving a prosthesis. The method includes the following: fixing a femoral trial component to the femur; coupling a reamer bushing relative to the femoral trial component; reaming a cavity into the femur using the reamer bushing as a guide; coupling at least one of a modular femoral box trial and a stem adapter relative to the femoral trial component; trialing the femoral trial component with the articulating surface of the femoral trial component; and performing the coupling of the reamer bushing, the reaming of the cavity, the coupling of the at least one of the modular femoral box trial and stem adapter, and the trialing of the femoral trial component all while the femoral trial component remains fixed to the distal femur.

A modular augment cone system and methods of implanting the modular augment cone system. The system includes a main body cone a first cutout in the cone wall, and including a proximal end, a distal end, and a cone wall extending between the proximal and distal ends. A portion of the cone wall proximal to the first cutout includes an attachment feature. A first augment cone is positionable in the first cutout, the first augment cone including an attachment feature configured to mate with the attachment feature of the cone wall to attach the first augment cone into the first cutout. The main body cone can include a second cutout in the cone wall. In such systems, the modular augment cone system can include a second augment cone configured to mate with an attachment feature of the cone wall to attach the second augment cone into the second cutout.

The method of treating osteoarthritis of the knee (OAK) includes resection of the patella, patellar tendon, proximal tibia, and distal femur, and bone grafting after resection. The bone grafting includes using a single complete osteo-articular allograft configured to replace the knee joint, distal femur, and proximal tibia. Metallic plates are used for internal fixation of the allograft. The procedure can provide patients with full knee flexion, and thereby enable kneeling, e.g., as required in the Islamic prayer.

The present disclosure relates to a tibial component for an endoprosthetic knee implant comprising a tibial baseplate and a keel extending from a lower surface of the tibial baseplate. The tibial baseplate is disposed at a keel posterior angle relative to the keel, and the tibial baseplate is also disposed at a keel varus angle relative to the keel. The disclosure further describes modular keel embodiments, exemplary instruments that can be used to implant exemplary tibial components into and onto the proximal tibia, methods related thereto, and kits therefore.

Examples of the invention relate to methods, implants, and instruments for compressing first and second bone portions or a bone portion and an implant together.

An orthopaedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient's knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient's knee to receive the implants. A method or technique for using the surgical instruments to prepare the bones is also disclosed.

According to one example, a tibial prosthesis that can include a tibial bearing component, tibial baseplate, an insert and a fastener. The tibial bearing component can have medial and lateral proximal articular surfaces and an opposing distal surface. The tibial bearing component can define at least one recess therein with the recess having an opening at a periphery of the tibial bearing component. The tibial baseplate can be coupled to the tibial bearing component on the proximal surface thereof and having a distal surface configured to be disposed on a resected proximal surface of a tibia. The insert can be configured to be disposed within the recess and can engage the tibial baseplate and the tibial bearing component. The fastener can be insertable into the tibial bearing component and can be configured to retain the insert to the tibial baseplate.

Augment element for knee prosthesis, comprising a metal body of a substantially truncated conical shape configured to be inserted into a bone extremity and having an outer surface comprising a metal trabecular surface. The metal body being hollow with an axial through-cavity defining a plurality of substantially annular transversal sections. The metal body is inclined in a direction of inclination, so as to define at least one eccentricity between a first transversal section at a first end of the axial through-cavity and a second transversal section at a second end of the axial through-cavity. The augment element further comprises a plurality of through-slits in the metal body, open from the first end up to an intermediate portion on the metal body, wherein the plurality of through-slits is configured for a radial compression of the metal body, locally reducing a circumference of the substantially annular transversal sections during insertion of the augment element, and increasing a press-fit towards a bone portion.

A tibial component of a knee prosthesis includes a tibial plate and a tibial insert, and anterior and posterior abutments projecting from an upper face of the tibial plate. The anterior abutment extends along at least part of the tibial plate and the posterior abutment extends for at least part of the tibial plate and comprises a part forming a promontory and an anterior cut-out, in particular central, in the form of a window formed in the anterior abutment opening onto the posterior face of the latter opposite the part forming the promontory. The tibial insert has a face upper, a face lower and a lateral face, which has a shape matching the part forming the promontory, characterised in that at least one flexible tab in the form of a hook projects centrally from an anterior face of the insert and locks by snap-fitting, into the anterior cut-out.

A knee prosthesis and a method of selecting for a particular patient a knee prosthesis from an inventory of available knee prosthesis or from 3D knee prosthesis models is provided. The method includes the steps of (a) parameterizing a knee prosthesis according to well-defined and independent knee joint compartments, (b) generating a large number knee shapes in the form of 3D knee prosthesis models which reproduce the 3D shape asymmetries of each individual knee, thereby enabling the replication of the knee motion of essentially any patient by generating shapes which vary the shape parameters (surface and dimension) of at least one of those compartments and storing these 3D knee prosthesis models in a database, and (c) studying the patient’s pathology and developing pre -pathological knee prosthesis criteria matching the patient’s needs. Using a planning algorithm, a suitable knee prosthesis may be selected among an inventory of existing knee prostheses or the large number of knee shapes, the prosthesis or shape selected best meeting the patient’s needs as determined by the study.