510(k) K242554 · HRS Plate, Fixation, Bone
Arthrex VAL and VAL KreuLock Compression Screw System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 21, 2024 |
| Received | Aug 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242554
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.