510(k) K884888 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent for Some Indications, Dec 29, 1988 |
| Received | Nov 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884888
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.