510(k) K871656 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
ORTHOMET AUSTIN-MOORE SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 9, 1987 |
| Received | Apr 28, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871656
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.