510(k) K243293 · MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Zimmer® Persona® Personalized Knee System
| Applicant | Zimmer Biomet, Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 20, 2024 |
| Received | Oct 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243293
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.