510(k) K221342 ยท HWC Screw, Fixation, Bone
REDEMPTION Beaming System
| Applicant | Vilex, LLC, Mcminnville TN, US |
| Decision | Substantially Equivalent, Dec 13, 2022 |
| Received | May 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221342
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.