510(k) K183383 · NKG Posterior Cervical Screw System
ANAX OCT Spinal System
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Dec 12, 2018 |
| Received | Dec 6, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183383
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.