510(k) K963309 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
APEX HOLE ELIMINATOR PS
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 12, 1996 |
| Received | Aug 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963309
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.