Clearance Summary
QEVO System with KINEVO 900 received FDA 510(k) clearance under submission number K170667, sponsored by Carl Zeiss Meditec, AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-08-18.
- Submission: K170667
- Applicant / Sponsor: Carl Zeiss Meditec, AG
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1480
- Decision date: 2017-08-18
Classification & Regulation
This clearance is catalogued under FDA product code GWG and 21 CFR 882.1480, within the Neurology review panel as a Class II device.