Clearance Summary
NUVO Implant System NUVO Instrument Kit Cases received FDA 510(k) clearance under submission number K202515, 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 General Hospital review panel. The statutory decision date of record is 2020-11-24.
- Submission: K202515
- Applicant / Sponsor: Jjgc Industria E Comercio DE Materiais Dentarios S.A.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6850
- Decision date: 2020-11-24
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.