Clearance Summary
LICOX IT2 COMPLETE BRAIN TUNNELING PROBE KIT received FDA 510(k) clearance under submission number K053244, sponsored by Integra Lifesciences Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2006-05-10.
- Submission: K053244
- Applicant / Sponsor: Integra Lifesciences Corp.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1620
- Decision date: 2006-05-10
Classification & Regulation
This clearance is catalogued under FDA product code GWM and 21 CFR 882.1620, within the Neurology review panel as a Class II device.