Clearance Summary
SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES received FDA 510(k) clearance under submission number K072672, sponsored by Abbott Spine, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-11-28.
- Submission: K072672
- Applicant / Sponsor: Abbott Spine, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2007-11-28
Classification & Regulation
This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.