510(k) K931333 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
ORTHOMET ACETABULAR CUP SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 14, 1994 |
| Received | Mar 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931333
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.