510(k) K853662 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
MUELLER CURVED STEM HEMI-PROSTHESIS
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 24, 1985 |
| Received | Sep 3, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853662
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.