510(k) K971705 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
IMPLEX HEP ACETABULAR CUP SYSTEM, CEMENTED
| Applicant | Implex Corp., Rockville MD, US |
| Decision | Substantially Equivalent, Aug 6, 1997 |
| Received | May 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971705
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.