510(k) K260624 ยท KWI Prosthesis, Elbow, Hemi-, Radial, Polymer
Arthrex Radial Head Replacement System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jul 30, 2026 |
| Received | Feb 26, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260624
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.