A tibial sample implant for use in knee joint replacement surgery has a lower part and an upper part. The upper part has a sliding surface designed to interact with a femoral component. A height adjustment mechanism can move the upper part in a guided manner relative to the lower part between a first position, in which the sliding surface is positioned at a first height above the lower part, and a second position, in which the sliding surface is positioned at a second height above the lower part. The height adjustment mechanism has a drive gear and a control cam. An output element is rotationally fixed to the upper part and has a support section supported on the control cam so that the upper part can be moved between the first position and the second position by a rotational movement of the drive gear.

A system and method for transmitting implant data includes an orthopedic implant, a wireless receiver, and a processing circuit electrically coupled to the wireless receiver. The orthopedic implant is configured to transmit implant identification data and implant sensor data to the wireless receiver in response to a power signal. The orthopedic implant may transfer the data over, for example, a wireless network. The processing circuit receives the implant identification data and the implant sensor data from the wireless receiver and is configured to retrieve patient-related data from a database based on the implant identification data. The processing circuit may also be configured to update a patient queue, assign a patient room to a patient, and/or transmit the patient-related data and the implant sensor data to a client machine located in the patient room.

A method of determining disc space geometry with the use of an expandable trial having endplate-mapping capabilities. An expandable trial is inserted into the disc space and its height is adjusted to obtain the desired decompression and spinal alignment (which is typically confirmed with the use of CT or Fluoroscopic imaging). The endplate dome/geometry dome is then determined by one of the following three methods: a) direct imaging through the trial, b) balloon moldings filled with flowable in-situ fluid (for example, silicon, polyurethane, or PMMA) from superior/inferior endplates or c) light-based imaging through superior & inferior balloons.

A tibial trial insert system includes a bearing component having a superior articulating surface for articulation with a distal femoral surface, a plate component having an inferior fixation surface for fixation to a proximal tibia, and an adjustment arrangement for adjusting a proximal/distal spacing between the bearing component and the plate component. The adjustment arrangement includes an adjustment device having a superior connector element that engages an inferior surface of the bearing component, an inferior base element adapted to be placed upon a superior surface of the plate component, and a telescopic mechanism coupled to the connector element and the base element. The telescopic mechanism can adjust a thickness of the adjustment device. At least one shim is insertable between the superior surface of the plate component and an inferior surface of the base element for adjusting a height level of the adjustment device relative to the plate component.

The disclosure provides example methods and non-transitory computer-readable mediums for acetabular cup placement. An example method includes a processor (a) determining for a first patient a sagittal acetabular cup position in the form of a standing AI, a seated AI and a SAA based on (i) a standing SS relative to a normative SS, (ii) a dSS between a standing position and an upright seated position, (iii) a femoral version corresponding to a femoral version outlier position, and (iv) a PFA to correspond to a PFA outlier position in a standing position or an upright seated position, (b) determining a coronal acetabular cup position in the form of a supine coronal anteversion and at least one of a supine or a standing coronal inclination based on the sagittal acetabular cup position, and (c) determining a post-operative standing AI and a post-operative seated AI based on the coronal acetabular cup position.

Various surgical impactors are disclosed. The surgical impactor may include a housing, a rod that extends at least partially inside the housing, a hammer head attached to the rod, and a hammer housing that receives the hammer head. Actuation of the rod can cause the hammer head to move proximally and/or distally inside, and to impact, the hammer housing. The force of the impact can be conveyed to a surgical implant, instrument, etc.