510(k) K954481 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
P.F.C. UNI-COMPARTMENTAL KNEE SYSTEM
| Applicant | Johnson & Johnson Professionals, Inc., Raritan NJ, US |
| Decision | Substantially Equivalent, Oct 10, 1996 |
| Received | Sep 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954481
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.