Clearance Summary
K3Pro Konus New Abutments and Implants received FDA 510(k) clearance under submission number K190192, sponsored by Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-02-10.
- Submission: K190192
- Applicant / Sponsor: Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2020-02-10
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.