A system for replacing at least a portion of a natural facet joint includes a fixation member implantable in a vertebra, an inferior facet articular surface and an inferior strut which may be formed separately from the inferior articular surface. The inferior strut has a first end securable to the fixation member and a second end which may comprise a sphere with a hemispherical surface. An attachment mechanism may include a capture feature shaped to receive the second end of the inferior strut, and the mechanism may provide an adjustable configuration, allowing polyaxial adjustment between the inferior articular surface and the second end. A locking member may be actuated to exert force on the second end to provide a locked configuration. The system may further include a superior facet joint implant with a superior articular surface shaped to articulate with the inferior articular surface.

One embodiment of the present disclosure provides a humeral implant. The humeral implant includes a tray including a body defining a bone facing recess and a liner recess, said bone facing recess including a ring surface and a convex surface, wherein the ring surface has a profile substantially corresponding to a profile of an outer ring of bone in an excision site of a patient; and wherein said convex surface has a profile substantially corresponding to a profile of a concave socket formed in the excision site. The humeral implant also includes a liner including a body defining a load bearing surface and a tray interface surface, said tray interface surface being configured to be at least partially received in said liner recess of said tray such that said implant is coupled to said tray.

The invention relates to a glenoid (shoulder socket) implant prosthesis, a humeral implant prosthesis, devices for implanting glenoid and humeral implant prostheses, and less invasive methods of their use for the treatment of an injured or damaged shoulder.

A dynamic trialing method generally allows a surgeon to perform a preliminary bone resection on the distal femur according to a curved or planar resection profile. With the curved resection profile, the distal-posterior femoral condyles may act as a femoral trial component after the preliminary bone resection. This may eliminate the need for a separate femoral trial component, reducing the cost and complexity of surgery. With the planar resection profile, shims or skid-like inserts that correlate to the distal-posterior condyles of the final insert may be attached to the distal femur after the preliminary bone resection to facilitate intraoperative trialing. The method and related components may also provide the ability of a surgeon to perform iterative intraoperative kinematic analysis and gap balancing, providing the surgeon the ability to perform necessary ligament and/or other soft tissue releases and fine tune the final implant positions based on data acquired during the surgery.

Devices, systems, and methods for a robot-assisted surgery. Navigable instrumentation, which are capable of being navigated by a surgeon using the surgical robot system, and navigation software allow for the navigated placement of interbody fusion devices or other surgical devices. The interbody implant navigation may involve navigation of access instruments (e.g., dilators, retractors, ports), disc preparation instruments, trials, and inserters.

Methods and systems for identifying and determining the size and orientation of a reamed portion of a patient's bone are disclosed. A tracking array and/or point probe may be inserted into an adapter device. The adapter device comprising a plurality of openings, having various connection means therein, such that when the tracking array is inserted into the adapter, a secure and robust connection is created. A reamer, stem, or similar tool may then be inserted into the opposing side of the adapter, during which, a secure and robust connection is created between the adapter and the tool. Thus, through the use of Computer Assisted Surgery Systems, a more accurate representation of the patient's anatomy can be obtained.

A method and system for guiding knee replacement procedures, the method comprising receiving first data values from one or more sensors and one or more functional measurement devices, performing a reference measurement based on the first data values from the one or more sensors and the one or more functional measurement devices prior to a femoral cut, generating joint replacement recommendations based on the reference measurement, receiving second data values from the one or more sensors and the one or more functional measurement devices, performing a control measurement based on the second data values from the one or more sensors and the one or more functional measurement devices after a femoral cut based on the joint replacement recommendations, receiving third data values from the one or more functional measurement devices, and performing a pressure test that measures loading, balance, and kinematic behavior at medial and lateral condyles based on the third data values.

An orthopaedic surgical instrument may include an elongated body with a proximal end and distal end. A clamp lever may be pivotally coupled to the proximal end of the elongated body. The clamp lever may be moveable between a locked position and an unlocked position. A biasing element may be configured to bias the clamp lever to the locked position.

A minimally invasive hip arthroplasty technique involves intramedullary insertion of an elongate femoral broach into a femur. The broach has a superior lateromedial transverse bore. A reaming rod is then located through the transverse bore and the neck of the femur. A cutting head is coupled to a distal end of the reaming rod via an incision. An orthogonal drive arm of an arthroplasty jig may also be inserted behind the cutting head to press the cutting head to ream the acetabulum while the reaming rod rotates the cutting head.

An orthopaedic surgical instrument system includes a tibial base trial and a tibial bearing trial. The tibial bearing trial is installed on the tibial base trial from the anterior side of the patient's tibia during an orthopaedic surgical procedure.