Clearance Summary
OPTIFLOW II FLOWABLE COMPOSITE, LC received FDA 510(k) clearance under submission number K130672, sponsored by Pac-Dent International, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-08-13.
- Submission: K130672
- Applicant / Sponsor: Pac-Dent International, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2013-08-13
Classification & Regulation
This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.