510(k) K870922 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
C.L.E. ACETABULAR CUP
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Oct 28, 1987 |
| Received | Mar 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870922
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.