K253195
- 510(k) number
- K253195
- Device name
- TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems
- Applicant
- ZheJiang Decans Medical Devices Co., Ltd. CN
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2026-06-02
- Date received
- 2025-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K253195.pdf
Official FDA record: K253195
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.