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# Enovis’ STAR Instrumentation for Ankle Replacement OK’d
- URL: https://www.fdaweb.com/enovis-star-instrumentation-for-ankle-replacement-okd/
- Published: 2022-12-01T12:00:00.000Z
- Updated: 2026-09-14T18:08:10.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5153302

FDA has approved an Enovis PMA for the STAR Patient Specific Instrumentation (STAR PSI System) and its use with the company’s STAR total ankle replacement system. The new device provides a personalized pre-operative plan for each patient, Enovis says, including a 3D visualization of the patient’s ankle joint along with information about any existing implants and bone defects, to plan for the total ankle replacement. The device is also intended to be used with an updated and simplified surgical technique, which has the potential to reduce operative time during total ankle replacement cases, the company says.