510(k) K001010 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ASCENT KNEE REVISION FEMORAL STEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Apr 27, 2000 |
| Received | Mar 29, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001010
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.