Spacer device for the two-phase treatment of infections of anatomic and reverse shoulder prostheses, including a humeral component equipped with a stem, a head component and means for connecting or articulating the humeral component with the head component.

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.

Example spinal implants and related apparatus and methods are disclosed. An example spinal implant includes an outer corpus and an inner corpus axially displaceably coupled to the outer corpus. A first lever accommodation is provided on the outer corpus and includes an elongated aperture. A first set of teeth are formed on a first side of the first lever accommodation. A second lever accommodation is provided on the inner corpus and includes an elongated aperture. A second set of teeth are formed on a second side of the second lever accommodation. The first and second lever accommodations are aligned. The example spinal implant includes a first guide on the inner corpus and a second guide on the outer corpus. The first and second guides allow for axial displacement of the inner corpus relative to the outer corpus and prevent rotation of the inner corpus relative to the outer corpus.

A method of fabricating a customized patient-specific guide block is disclosed. The method includes generating a image of a patient's bony anatomy and an implanted prosthetic component secured to the patient's bony anatomy, identifying landmarks on the patient's bony anatomy and the prosthetic component, selecting a revision surgical instrument based the image and the landmarks, and manufacturing the customized patient-specific guide block including a customized prosthesis-specific negative contour shaped to match a corresponding contour of the implanted prosthetic component.

A method of revising a patient having a fusion cage implanted within a spinal column, involving percutaneously delivering a first end of a tube to the spinal column, fluidly connecting the first end of the tube to the fusion cage, and delivering a bone growth agent into the fusion cage through the tube.

A humeral anchor assembly is provided that includes a humeral anchor and at least one screw. The humeral anchor is configured to form a part of or support a part of a shoulder prosthesis. The humeral anchor has a distal portion configured to be anchored in a proximal region of a humerus and a proximal portion. The proximal portion includes a proximal face configured to engage an articular component within a periphery thereof. The proximal portion also includes at least one aperture disposed adjacent to the periphery. The at least one screw is disposed through the at least one aperture. The screw has a first end portion engaged with the proximal portion of the anchor and a second end portion disposed in or through cortical bone of the humerus.

An orthopaedic surgical instrument includes a cup including an outer surface having an opening positioned on a component-engaging side and an inner wall extending from the opening of the outer surface to a back wall. The inner wall having a plurality of stepped surfaces facing the component-engaging side. Each of the plurality of stepped surfaces is sized to receive a platform of a tibial tray.

Methods and systems for retention and use of historical patient-specific information in selecting and/or designing patient-adapted articular repair systems are disclosed herein. Various embodiments include articular repair system components that are selected and/or designed based, at least in part, on both current patient-specific information and historical patient-specific information. According to certain embodiments, a method of making an implant component for intended treatment of a diseased or damaged joint of a patient is disclosed.

An implant assembly may include a first component having a proximal plate and a distal portion extending from the proximal plate, a first screw of a first type, and a first screw of a second type. The proximal plate may have a proximal face, a distal face configured to abut bone, and a periphery. The proximal plate may define a plurality of apertures. An opening may be defined by the proximal plate and extend through the distal portion. Each of the plurality of apertures may be disposed between the opening and the periphery. The first screw of the first type may be sized and configured to be received in the opening and engage bone. The first screw of the second type may be sized and configured to be received in at least one of the plurality of apertures.

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.