510(k) K984054 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
AGC V2 REVISION KNEE SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 30, 1999 |
| Received | Nov 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984054
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.