Clearance Summary
BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES received FDA 510(k) clearance under submission number K100785, sponsored by Bonart Co., 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 2010-12-03.
- Submission: K100785
- Applicant / Sponsor: Bonart Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2010-12-03
Classification & Regulation
This clearance is catalogued under FDA product code EBW and 21 CFR 872.4200, within the Dental review panel as a Class I device.