510(k) K962468 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
HEDROCEL ACETABULAR RESTRICTOR
| Applicant | Implex Corp., Rockville MD, US |
| Decision | Substantially Equivalent, Feb 3, 1997 |
| Received | Jun 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962468
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.