510(k) K251725 · NKG Posterior Cervical Screw System
ANAX OCT Spinal System
| Applicant | Cg Medtech Co., Ltd., Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Jun 25, 2025 |
| Received | Jun 5, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251725
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.