510(k) K960180 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
22 MM COCR HEAD & POLYETHLENE LINER
| Applicant | Stelkast Company, Pittsburgh PA, US |
| Decision | Substantially Equivalent, May 2, 1996 |
| Received | Jan 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960180
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.