510(k) K961021 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
KIRSCHNER KNEE MODIFIED
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Mar 17, 1997 |
| Received | Mar 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961021
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.