510(k) K211768 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
LINK Endo-Model Knee System, Femoral Segments (Augments), UHMWPE
| Applicant | Waldemar Link GmbH & Co. KG, Norderstedt, DE |
| Decision | Substantially Equivalent, Jun 30, 2021 |
| Received | Jun 8, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211768
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.