K250866
- 510(k) number
- K250866
- Device name
- Sovereign Posterior Cervical System
- Applicant
- Met One Technologies, LLC TX · US
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2025-05-20
- Date received
- 2025-03-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K250866.pdf
Official FDA record: K250866
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.