510(k) K151938 ยท NKG Posterior Cervical Screw System
S4 Cervical Spinal and Occiput Systems
| Applicant | Aesculap Implant Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Oct 21, 2015 |
| Received | Jul 14, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151938
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.