Clearance Summary
PRELUDE II TOUNGE SUSPENSION SYSTEM received FDA 510(k) clearance under submission number K103179, sponsored by Siesta Medical, 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 2010-12-20.
- Submission: K103179
- Applicant / Sponsor: Siesta Medical, Inc.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2010-12-20
Classification & Regulation
This clearance is catalogued under FDA product code ORY and 21 CFR 872.5570, within the Dental review panel as a Class II device.