A device, a system and a method for determining an anteversion angle of a femoral shaft of a femur are provided. The device includes a provision unit and a processing unit. The provision unit is configured to provide image data of the femur, and wherein the processing unit is configured to determine a longitudinal shaft axis extending through the femoral shaft based on the image data. The processing unit is further configured to determine at least two landmarks of the femur based on the image data, and place a tangent trough each landmark parallel to the shaft axis. The processing unit is configured to determine the anteversion angle of the femoral shaft based on the tangents and the shaft axis of the femoral shaft.

The instrumentation aims at improving the implantation of a glenoidal prosthetic component which is both provided with a convex articular surface defining a joint axis and intended to articulate with a humeral prosthetic component, and which is adapted so as to be fixedly assembled with a plate to be anchored to the glenoid, the assembly between the glenoidal prosthesis component and the plate being centered on an implantation axis which is both parallel and shifted relatively to the joint axis, the relative position of the glenoidal prosthesis component and of the plate being adjustable around the implantation axis before fixing the assembly. The instrumentation comprises a tool for positioning the glenoidal prosthetic component and the plate relatively to each other angularly around the implantation axis, this tool comprising a body, which, in use, extends transversely to the implantation axis and which is provided with localization elements for localizing an implantation angle centered on the implantation axis, so that the tool is able to intra-operatively protract the implantation angle with respect to the glenoid.

An orthopedic device includes a monolithic patient-specific guide. The patient-specific guide includes a three-dimensional contact surface preoperatively configured from medical scans of a specific patient as a negative surface of a medial portion of a proximal femoral bone of the patient according to a preoperative surgical plan for the patient. The guide also includes a proximal planar surface configured for guiding a resection of a femoral neck of the patient, and a scale formed on the planar surface. The scale is configured for indicating a preoperatively planned femoral version of a femoral stem implant and deviations therefrom.

An orthopedic surgical instrument and method for positioning an acetabular prosthetic component in a patient's surgically-prepared acetabulum is disclosed. The orthopedic surgical instrument has a base configured to engage the patient's pelvis, a first linkage pivotally coupled to the base, a locking mechanism operable to lock the first linkage in position relative to the base, and a second linkage removably coupled to the first linkage. The second linkage has an alignment axis corresponding to a desired abduction angle and a desired anteversion angle of the acetabular axis of the acetabular prosthetic component.

A neck trial (170) is disclosed. The neck trial has a body (182) and a neck (186). The body has an exterior surface. The neck extends away from the body along a neck axis (190). At least one first line (194) is provided on the exterior surface, which extends in a first direction parallel to an inferior-superior axis of a patient when in use. At least one second line (196) is provided on the exterior surface, which extends in a second direction parallel to a medial-lateral axis of the patient in use. The number of first lines, or the position of the first line or lines relative to the second line or lines, is indicative of an amount of offset in the medial-lateral direction caused by the neck trial. The number of second lines, or the position of the second line or lines relative to the first line or lines, is indicative of an amount of leg-length in the inferior-superior direction caused by the neck trial. A kit of parts, a trial assembly and a method of trialling a joint of a patient are also disclosed.

Embodiments of the invention include devices and methods for implanting arthroplasty devices. Some embodiments include designs that allow for use of x-ray images as the only images used to fully and accurately preoperatively and intraoperatively size and align arthroplasty device components and prepare all necessary tissue.

Direct anterior approach (DAA) with the patient lying supine has facilitated the use of intraoperative fluoroscopy and allows for standardized positioning of the patient. The method disclosed herein uses intraoperative fluoroscopy to measure acetabular component anteversion and more particularly, a method for measuring/calculating intraoperative cup (acetabular component) anteversion is provided based on the measured acetabular component abduction angle and a c-arm tilt angle (CaT).

Disclosed herein is a balancer algorithm to perform joint balancing calculations to identify target solutions based on surgeon preference. The balancer algorithm can generate a suggested final implant plan from a predetermined range. The balancer algorithm can be used in a knee arthroplasty procedure to generate bone resection depths, bone gaps, implant angulations, required soft tissue release, etc. Input to the balancer algorithm can include preoperative data, intraoperative data, and surgeon preference data.

Embodiments of a system and method for assessing hip arthroplasty component movement are generally described herein. A method may include receiving data from a sensor embedded in a femoral head component, the femoral head component configured to fit in an acetabular component, determining information about a magnetic field from the data, and outputting an indication of an orientation, coverage, or a force of the femoral head component relative to the acetabular component.

A surgical driver apparatus includes a housing and an inner driver shaft having a proximal end secured within the housing and a distal end extending out from a first side of the housing. The inner driver shaft is configured to rotate with respect to the housing. The surgical driver apparatus further includes an outer driver shaft and an idler driver shaft. The outer driver shaft is positioned coaxial with the inner driver shaft and configured to rotate independently from the inner driver shaft. The idler driver shaft is configured to transmit torque to the outer driver shaft. Additionally, the surgical driver apparatus includes a driver key comprising a driving feature and a counter-driving feature. The driver key is configured to engage a second side of the housing in one of a plurality of orientations configured to rotate the inner driver shaft and/or the outer driver shaft.