Clearance Summary
PORTA MAXIMUM, MODEL# 2066 received FDA 510(k) clearance under submission number K012835, sponsored by Wieland Edelmetalle GmbH & Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-11-01.
- Submission: K012835
- Applicant / Sponsor: Wieland Edelmetalle GmbH & Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 2001-11-01
Classification & Regulation
This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.