510(k) K234044 · JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ACS® LD FB Knee System
| Applicant | Implantcast GmbH, Buxtehude, DE |
| Decision | Substantially Equivalent, Sep 6, 2024 |
| Received | Dec 21, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234044
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.