510(k) K012348 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
MAXIM RPG PS FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 15, 2001 |
| Received | Jul 24, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012348
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.