Clearance Summary
PATHFINDER SYSTEM POLYAXIAL PEDICLE SCREWS received FDA 510(k) clearance under submission number K071174, 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 2007-07-25.
- Submission: K071174
- Applicant / Sponsor: Abbott Spine, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2007-07-25
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.