Clearance Summary
TMJ CANNULA SET received FDA 510(k) clearance under submission number K871648, sponsored by Aspen Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1987-06-08.
- Submission: K871648
- Applicant / Sponsor: Aspen Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4120
- Decision date: 1987-06-08
Classification & Regulation
This clearance is catalogued under FDA product code DZI and 21 CFR 872.4120, within the Dental review panel as a Class II device.