510(k) K896105 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
EVOLUTION HIP SYSTEM
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Dec 29, 1989 |
| Received | Oct 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896105
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.