510(k) K242412 · MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Agility Symmetric Total Knee System
| Applicant | Medisurge, LLC, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Nov 6, 2024 |
| Received | Aug 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242412
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.