510(k) K221031 ยท HSB Rod, Fixation, Intramedullary And Accessories
Arthrex DualCompression Hindfoot Fusion Nail Implant System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 20, 2022 |
| Received | Apr 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221031
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.