Clearance Summary
Novidia Flowable Composite received FDA 510(k) clearance under submission number K182580, sponsored by Nobio , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-07-03.
- Submission: K182580
- Applicant / Sponsor: Nobio , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2019-07-03
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.