Clearance Summary
AURAGEN CORTICAL SURFACE ELECTRODES received FDA 510(k) clearance under submission number K082250, sponsored by Integra Neurosciences. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2008-10-10.
- Submission: K082250
- Applicant / Sponsor: Integra Neurosciences
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1310
- Decision date: 2008-10-10
Classification & Regulation
This clearance is catalogued under FDA product code GYC and 21 CFR 882.1310, within the Neurology review panel as a Class II device.