Clearance Summary
COLUMBIA 600 ELECTRODE, COLUMBIA 06 LEADWIRE received FDA 510(k) clearance under submission number K080386, sponsored by Columbia Scientific Development, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2008-05-30.
- Submission: K080386
- Applicant / Sponsor: Columbia Scientific Development, LLC
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 2008-05-30
Classification & Regulation
This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.