510(k) K223852 · NKG Posterior Cervical Screw System
VySpan PCT System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Feb 24, 2023 |
| Received | Dec 22, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223852
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.