510(k) K972401 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
HOWMEDICA MODULAR REPLACEMENT SYSTEM - DISTAL FEMORAL/PROXIMAL TIBIAL SEGMENTS
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Jul 13, 1998 |
| Received | Jun 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972401
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.