Clearance Summary
Neodent Implant System-Helix NGM Compact Surgical Kit Cases received FDA 510(k) clearance under submission number K214051, sponsored by JJGC Indústria e Comércio de Materiais Dentários S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2022-04-13.
- Submission: K214051
- Applicant / Sponsor: JJGC Indústria e Comércio de Materiais Dentários S.A.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6850
- Decision date: 2022-04-13
Classification & Regulation
This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.