510(k) K160697 · NKG Posterior Cervical Screw System
Gibralt® Spine System and Gibralt® Occipital Spine System
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Jun 28, 2016 |
| Received | Mar 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160697
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.