510(k) K892394 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent for Some Indications, Jul 19, 1989 |
| Received | Apr 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892394
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.