510(k) K240299 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Persona the Personalized Knee System (Persona OsseoTi 3-Peg Patella)
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Apr 26, 2024 |
| Received | Feb 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240299
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.