510(k) K242543 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 22, 2024 |
| Received | Aug 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242543
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.