Clearance Summary
SURPASS received FDA 510(k) clearance under submission number K061981, sponsored by Apex Dental Materials, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-07-31.
- Submission: K061981
- Applicant / Sponsor: Apex Dental Materials, Inc.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 2006-07-31
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.