510(k) K890054 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
M.E.M. ACETABULAR CUP W/SULMESH FOR CEMENT APPLI.
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent for Some Indications, Feb 8, 1989 |
| Received | Jan 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890054
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.