Clearance Summary
Neodent Implant System GM Line received FDA 510(k) clearance under submission number K173902, 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 2018-04-20.
- Submission: K173902
- 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 872.3630
- Decision date: 2018-04-20
Classification & Regulation
This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.