510(k) K200709 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Kyocera Bipolar Hip System
| Applicant | Kyocera Medical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Apr 17, 2020 |
| Received | Mar 18, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200709
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.