Clearance Summary
PLANMECA PROMAX 3D MID received FDA 510(k) clearance under submission number K103689, sponsored by Planmeca Oy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-03-17.
- Submission: K103689
- Applicant / Sponsor: Planmeca Oy
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1800
- Decision date: 2011-03-17
Classification & Regulation
This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.