510(k) K230120 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
KeYi Total Knee System
| Applicant | Beijing Keyi Medical Device Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Apr 19, 2024 |
| Received | Jan 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230120
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.