510(k) K190122 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Renovis A200 PS Knee System as part of the Renovis A200 Knee System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Jun 20, 2019 |
| Received | Jan 25, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190122
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.