Clearance Summary
MAXIBOND received FDA 510(k) clearance under submission number K884575, sponsored by Ortho Source. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-01-03.
- Submission: K884575
- Applicant / Sponsor: Ortho Source
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3750
- Decision date: 1989-01-03
Classification & Regulation
This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.