510(k) K892059 ยท LZY Prosthesis, Hip, Hemi-, Femoral, Metal Ball
FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jul 19, 1989 |
| Received | Mar 29, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892059
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.