510(k) K203595 ยท HWC Screw, Fixation, Bone
DynaFuse Fixation System
| Applicant | MedShape, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Jan 4, 2022 |
| Received | Dec 9, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203595
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.