510(k) K182182 ยท NKG Posterior Cervical Screw System
YUKON OCT Spinal System
| Applicant | K2m, Leesburg VA, US |
| Decision | Substantially Equivalent, Nov 15, 2018 |
| Received | Aug 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182182
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.