510(k) K153370 ยท NKG Posterior Cervical Screw System
Caspian OCT/MESA Mini/DENALI Mini Spinal System
| Applicant | K2m, Incorporated, Leesburg VA, US |
| Decision | Substantially Equivalent, Feb 16, 2016 |
| Received | Nov 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153370
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.