510(k) K213394 · NKG Posterior Cervical Screw System
Vy Spine VySpan PCT System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Dec 10, 2021 |
| Received | Oct 15, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213394
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.