510(k) K150570 ยท NKG Posterior Cervical Screw System
ANAX OCT Spinal System
| Applicant | U&I Corporation, Uijeongbu-Si, Gyeonggi-Do, KR |
| Decision | Substantially Equivalent, Jun 3, 2015 |
| Received | Mar 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150570
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.