510(k) K904205 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
AMK MODULAR TIBIAL WEDGE SYSTEM
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Oct 22, 1990 |
| Received | Sep 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904205
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.