510(k) K222799 · HWC Screw, Fixation, Bone
Haymaker® Screw System
| Applicant | Orthocircle Spine D.B.A. OC Medical Devices, Savannah GA, US |
| Decision | Substantially Equivalent, Jan 10, 2023 |
| Received | Sep 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222799
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.