An expandable augment system is provided for use with an acetabular cup. The expandable augment system can include an expandable augment module that is adjustable in size and that can be adjusted incrementally between a fully collapsed state and an expanded state. A first portion of the expandable augment module is attachable to an outer surface of an acetabular cup and a second portion of the expandable augment module is attachable to bone or to a fixed augment module (e.g., a fixed angle augment module) that is attached to bone and interposed between the adjustable augment module and bone.

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.

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.

An implant, a fitting plate suitable for placing of an implant, and a method for manufacturing an implant suitable for application on one or more bones.

Methods and systems of augmenting an implant intraoperatively and preparing a cone for revision surgical procedure are disclosed. A system includes a cutting device, a tracking and navigation system and a cutting system in operable communication with the cutting device and the tracking and navigation system. The cutting device includes a communication system, a cutting element, and a plurality of optical trackers. The tracking and navigation system is configured to detect a location of optical trackers. The control system is configured to cause the tracking and navigation system to detect the location of the cutting device, determine a revised shape for an implant cavity, cause the cutting device to cut the implant cavity to the revised shape, select a shape for a cone to be placed in the revised implant cavity, and machine the cone to the selected shape.

The present invention relates to an implant (1) for the correction of gleno-humeral instability, in particular for the correction of a glenoid defect (Dg) of the glenoid (G) of a patient, said implant (1) having a substantially flat portion (3), said substantially flat portion (3) being suitable, when said implant (1) is in use, for being placed at the site of the glenoid defect (Dg) in contact with the external bone portion of the glenoid (G) of a patient, said implant (1) being characterized in that at least said flat portion (3) is made of heterologous deproteinized bone material.

The present disclosure relates to the field of medical instruments, in particular to a pad for acetabular bone revision and reconstruction and a fixing structure for a pad and an acetabular cup prosthesis. The pad is located between an acetabular cup prosthesis and the acetabular bone, and is connected to the acetabular cup prosthesis and the acetabular bone respectively. The pad includes a first component and a second component which has the same or different radius and shape as or from the radius and shape of the first component; the first component is movably connected with the second component; and the shape of the connected first component and second component is matched with a defective part of the acetabular bone.

An orthopaedic surgical instrument system includes a first broach including a first end configured to be separately secured to a handle and a tapered body having a plurality of cutting teeth defined therein, and a second broach including a first end configured to be separately secured to the handle in place of the first broach, a first tapered body extending distally from a second end positioned opposite the first end, and a second tapered body extending distally from the first tapered body. The tapered body of the first broach and the first tapered body of the second broach have a first outer geometry and the second tapered body has a second outer geometry different from the first outer geometry.

A surgical implant includes a hemispherical cup having a bone-abutment exterior surface defining a convex side of the hemispherical cup and an interior surface defining a concave side of the hemispherical cup with a cavity, and a stress-diffusion element extending directly from the bone-abutment exterior surface of the hemispherical cup at an anteverted orientation to the hemispherical cup. The implant may further include at least one aperture defined by a circumferential surface extending between the bone-abutment exterior surface and the interior surface, the at least one aperture operable to receive a screw therethrough.

The present application relates to the technical field of biomaterials for implant and intervention, and particularly to a total knee joint prosthesis for revision after a unicompartmental knee arthroplasty including a tibial plateau and a tibial pad mounted on the tibial plateau; the tibial plateau includes an installation platform and an installation column fixedly connect to a side of the installation platform; a filling block is provided on a side of the installation platform towards the installation column; and the filling block is configured to be placed at a side of the human tibia where a unicompartmental knee arthroplasty is performed.