510(k) K243174 ยท OYK Ankle Arthroplasty Implantation System
Cadence Ankle PSI System
| Applicant | 3D Systems, Inc., Littleton CO, US |
| Decision | Substantially Equivalent, Oct 25, 2024 |
| Received | Sep 30, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243174
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.