Clearance Summary
True Function Adjustable Herbst Appliances received FDA 510(k) clearance under submission number K170578, sponsored by True Function Laboratory, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-11-24.
- Submission: K170578
- Applicant / Sponsor: True Function Laboratory, Inc.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2017-11-24
Classification & Regulation
This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.