510(k) K260809 · HWC Screw, Fixation, Bone
Arthrex Sterile VAL and VAL KreuLock Compression Screw System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jun 25, 2026 |
| Received | Mar 12, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260809
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.