510(k) K180851 · NKG Posterior Cervical Screw System
VERTEX Reconstruction System
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Apr 18, 2018 |
| Received | Apr 2, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180851
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.