Clearance Summary
Neodent Implant System GM Line received FDA 510(k) clearance under submission number K180536, sponsored by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2018-08-30.
- Submission: K180536
- Applicant / Sponsor: Jjgc Industria E Comercio DE Materiais Dentarios S.A.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2018-08-30
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.