510(k) K252196 ยท HSB Rod, Fixation, Intramedullary And Accessories
Arthrex FibuLock Nail System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 5, 2026 |
| Received | Jul 14, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252196
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.