510(k) K232114 · HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
TRIBRID® Unicompartmental Knee System
| Applicant | Kyocera Medical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Apr 4, 2024 |
| Received | Jul 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232114
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.