510(k) K172524 ยท 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 17, 2018 |
| Received | Aug 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172524
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.