510(k) K173656 ยท HSB Rod, Fixation, Intramedullary And Accessories
Arthrex FibuLock Nail
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jul 26, 2018 |
| Received | Nov 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173656
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.