510(k) K902137 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
P.F.C. HIP SYSTEM NON-POROUS ACETABULAR COMPONENT
| Applicant | Johnson & Johnson Orthopaedics, Inc., Braintree MA, US |
| Decision | Substantially Equivalent, Jun 26, 1990 |
| Received | May 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902137
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.