Clearance Summary
LORENZ BLUE DEVICE received FDA 510(k) clearance under submission number K020407, sponsored by Walter Lorenz Surgical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-02-22.
- Submission: K020407
- Applicant / Sponsor: Walter Lorenz Surgical, Inc.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4760
- Decision date: 2002-02-22
Classification & Regulation
This clearance is catalogued under FDA product code MQN and 21 CFR 872.4760, within the Dental review panel as a Class II device.