510(k) K260697 · KWQ Appliance, Fixation, Spinal Intervertebral Body
VyPlate Anterior Cervical Plate System
| Applicant | Vy Spine, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Mar 27, 2026 |
| Received | Mar 4, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260697
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.