Clearance Summary
MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL received FDA 510(k) clearance under submission number K060270, sponsored by Linvatec Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-04-10.
- Submission: K060270
- Applicant / Sponsor: Linvatec Corp.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4120
- Decision date: 2006-04-10
Classification & Regulation
This clearance is catalogued under FDA product code DZI and 21 CFR 872.4120, within the Dental review panel as a Class II device.