510(k) K222653 · NJD Prosthesis, Knee, Femorotibial, Unicompartmental/Unicondylar, Uncemented, Porous-Coated, Metal/Polymer
JOURNEY II UK and ENGAGE Cementless Partial Knee System
| Applicant | Smith+Nephew, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 28, 2022 |
| Received | Sep 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222653
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.