K231658
- 510(k) number
- K231658
- Device name
- VEOS Spinal Fixation System
- Applicant
- Spineway FR
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2023-10-10
- Date received
- 2023-06-07
- 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: K231658.pdf
Official FDA record: K231658
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.