510(k) K251840 · MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Zimmer® Persona® Personalized Knee System
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 28, 2026 |
| Received | Jun 16, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251840
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.