510(k) K240669 · JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ACTIFY 3D Total Knee System, ACTIFY Total Knee System
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jun 20, 2024 |
| Received | Mar 11, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240669
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.