K260697
- 510(k) number
- K260697
- Device name
- VyPlate Anterior Cervical Plate System
- Applicant
- Vy Spine, LLC UT · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2026-03-27
- Date received
- 2026-03-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K260697.pdf
Official FDA record: K260697
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.