510(k) K945783 ยท JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
ORTHOMET TITANIUM HYBRID FEMORAL STEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 30, 1995 |
| Received | Nov 25, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945783
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.