K233078
- 510(k) number
- K233078
- Device name
- Posterior Cervical Spine System
- Applicant
- Double Medical Technology, Inc. CN
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2023-11-22
- Date received
- 2023-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233078.pdf
Official FDA record: K233078
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.