510(k) K082500 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
DEPUY SIGMA CR-F FEMORAL COMPONENT
| Applicant | DePuy Orthopaedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 18, 2008 |
| Received | Aug 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082500
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.