510(k) K223392 ยท HWC Screw, Fixation, Bone
REVCON (TM) Screw System
| Applicant | Voom Medical Devices, Inc., New York City NY, US |
| Decision | Substantially Equivalent, Feb 28, 2023 |
| Received | Nov 8, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223392
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.