Clearance Summary
Vent-Os Sinus Dilation family received FDA 510(k) clearance under submission number K160770, sponsored by Sinusys Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2016-06-29.
- Submission: K160770
- Applicant / Sponsor: Sinusys Corporation
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 2016-06-29
Classification & Regulation
This clearance is catalogued under FDA product code LRC and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.