510(k) K031804 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
COMPRESS DISTAL FEMORAL REPLACEMENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 18, 2003 |
| Received | Jun 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031804
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.