510(k) K241592 · HWC Screw, Fixation, Bone
Arthrex VAL and VAL KreuLock Compression Screw System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 31, 2024 |
| Received | Jun 3, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241592
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.