Clearance Summary
MODIFICATION TO VERTE-STACK SPINAL SYSTEM received FDA 510(k) clearance under submission number K062133, sponsored by Medtronic Spinal and Biologics Div. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-09-26.
- Submission: K062133
- Applicant / Sponsor: Medtronic Spinal and Biologics Div
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2006-09-26
Classification & Regulation
This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.