510(k) K925072 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
AMK LANDMARK REVISION KNEE SYSTEM
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 21, 1994 |
| Received | Oct 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925072
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.