K251725
- 510(k) number
- K251725
- Device name
- ANAX OCT Spinal System
- Applicant
- Cg Medtech Co., Ltd. KR
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2025-06-25
- Date received
- 2025-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K251725.pdf
Official FDA record: K251725
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.