510(k) K221572 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
VyPlate Anterior Cervical Plate System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Jul 26, 2022 |
| Received | Jun 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221572
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.