Clearance Summary
MODIFICATION TO ENTELLUS MEDICAL RS-SERIES SYSTEM received FDA 510(k) clearance under submission number K081542, sponsored by Entellus Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2008-06-27.
- Submission: K081542
- Applicant / Sponsor: Entellus Medical, Inc.
- Clearance pathway: Special
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 2008-06-27
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.