A61F2/3859

Augmented Reality Display Systems for Fitting, Sizing, Trialing and Balancing of Virtual Implant Components on the Physical Joint of the Patient
20230038678 · 2023-02-09 ·

Devices and methods for performing a surgical step or surgical procedure with visual guidance using an optical head mounted display are disclosed.

Patient specific bone preparation for consistent effective fixation feature engagement
11491016 · 2022-11-08 · ·

An optimized press-fit between a resected bone and an articular implant may, for instance, reduce undesirable qualities, including excess micromotion, stress transmission, and/or strain. By taking into account heterogeneous bone properties, the parameters of a bone resection can be determined as to optimize the press-fit between a resected bone and an articular implant. An optimized press-fit is obtained by determining ideal engagement characteristics corresponding to the fit between the fixation features of an articular implant and a bone. Then, taking into account a bone's heterogeneous properties, the parameters of a bone resection that would substantially achieve the determined ideal engagement characteristics are determined.

COMPOSITE ORTHOPAEDIC PROSTHESIS AND METHOD OF MAKING THE SAME

An orthopaedic prosthesis includes a femoral component comprising polymeric materials. The polymeric materials may include a polyaromatic ether or a polyacetal. The orthopaedic prosthesis may include a component having an articular layer and a support layer adjacent the articular layer. The support layer may include a reinforcement fiber. The orthopaedic prosthesis may be a knee prosthesis.

Mould for making a temporary prosthetic component for a knee

Described is a mould (1) for making a temporary prosthetic component for a knee in an operating room comprising: a first half-mould (10); a second half-mould (20) which can be coupled to the first half-mould (10) for forming a moulding chamber (C) for a temporary prosthetic component made of medical cement; and elements (30) for fixing the first half-mould (10) to the second half-mould (20). Each fixing element (30) has a rod (31) configured for connecting the first half-mould (10) to the second half-mould (20) and defining a weakness neck (32) configured to allow a facilitated breakage of the rod (31).

Augment and means for connecting the same to a joint prosthesis
11491013 · 2022-11-08 · ·

An orthopedic system includes an augment that includes a proximal surface and a distal surface, a recessed slot extending along the distal surface, and a through-bore extending between the proximal and distal surfaces and intersecting the slot. The system also includes a coupling component that includes a head and a body. The head has an aperture and is configured to be slidingly received by the recessed slot wherein, when the head is received within the recessed slot, the aperture aligns with the through-bore. The system further includes a femoral prosthesis that has an articular side that defines condylar portions and a bone facing side opposite the articular side. The bone facing side defines a coupling bore. The coupling bore is configured to receive the body of the coupling component for connection thereto.

Tibial cut guide
11571224 · 2023-02-07 · ·

Methods and apparatuses including apparatuses that can be used for guiding resection of a tibia during a knee replacement surgery procedures are disclosed. According to one example, an apparatus for guiding a tibial bone cut during knee replacement surgery is disclosed. The apparatus can comprise a first portion and a second portion. The first portion can be configured to position the apparatus relative to one or more of a medial condyle of a femur, a lateral condyle of the femur, a medial condyle of a femoral component and a lateral condyle of the femoral component. The second portion can be connected to the first portion and can define one or more slots. The slots can be configured for at least one of a first proximal cut and a first sagittal cut to the tibia.

METALLIC ORTHOPAEDIC IMPLANT AND METHOD OF MAKING THE SAME
20230096615 · 2023-03-30 ·

An orthopaedic implant includes a femoral component having a metallic zirconium and niobium coating disposed therein. A method of making the femoral component using direct energy deposition or co-molding is also disclosed.

Orthopaedic surgical instrument system and a method of trialing an orthopaedic prosthetic assembly

An orthopaedic surgical instrument system includes a hinged tibial insert trial and a tibial base trial. A post adapter is sized to be positioned over a post of the tibial base trial and to be positioned in a central opening defined in the hinged tibial insert trial. The hinged tibial insert trial includes a housing configured to be received in a femoral component and a button mechanism to selectively secure the hinged tibial insert trial to the femoral component. The system may include a shim trial sized to be attached to an inferior surface of the hinged tibial insert trial.

PATELLAR IMPLANT

In accordance with one or more embodiments herein, a patellofemoral implant arrangement 200 for repairing damage in a patellofemoral articulation of a patient is provided. The patellofemoral implant arrangement 200 comprises a femoral trochlear implant 250, comprising an articulating surface 255, and a patellar implant 300, configured to be inserted, preferably with press-fit, into a recess 620 in a patella 600 in such a way that the perimeter of an articulating surface 310 of the patellar implant 300 does not extend beyond a surrounding articulating surface of the patella 600. The articulating surfaces 255, 310 of the femoral trochlear implant 250 and the patellar implant 300 are designed to allow that they at least partly interact with each other when the implants 250, 300 are implanted into the knee joint and the patella 600 lies in the intercondylar groove of the femur. Preferably, the articulating surface 255 of the femoral trochlear implant 250 is a metal or ceramic surface; and the articulating surface 310 of the patellar implant 300 is not a metal or ceramic surface. The articulating surface 310 of the patellar implant 300 may be designed to correspond to the curvature of a simulated healthy articulating surface of the undamaged patella 600 at the site of diseased cartilage. The contour curvature of the articulating surface 310 may be generated based on the determined surface curvature of the cartilage and/or the subchondral bone in a predetermined area comprising and surrounding the site of diseased cartilage and/or bone in the patella 600, to mimic the original, undamaged, articulating surface of the patella 600.

Knee prosthesis
11612487 · 2023-03-28 ·

A knee prosthesis comprises a femoral component for securement to a femur, the femoral component defining medial and lateral J-shaped condyles and an intercondylar groove; and a fixed bearing tibial component for securement to a tibia, the tibial component having respective bearing surfaces which are fixed with respect to both a tibial engaging component and a stabilising peg for securing the tibial component to a tibia, the respective bearing surfaces being shaped to engage with said condyles both when the knee, in use, is extended and also over a range of flexion.