510(k) K231649 ยท HWC Screw, Fixation, Bone
Intraosseous Fusion Device System
| Applicant | Auxano Medical, LLC, Brecksville OH, US |
| Decision | Substantially Equivalent, Sep 29, 2023 |
| Received | Jun 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231649
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.