510(k) K884789 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent for Some Indications, Feb 8, 1989 |
| Received | Nov 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884789
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.