510(k) K864671 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ANATOMIC MODULAR KNEE (AMK) SYSTEM
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Feb 6, 1987 |
| Received | Dec 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864671
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.