510(k) K183583 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Vanguard Complete Knee System
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 10, 2019 |
| Received | Dec 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183583
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.