510(k) K872019 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
BI-ARTICULAR II HIP DEVICE
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 21, 1987 |
| Received | May 26, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872019
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.