30
Participants
Start Date
December 1, 2018
Primary Completion Date
July 18, 2019
Study Completion Date
July 18, 2019
ClariFix
The ClariFix™ device (K162608) is an FDA 510(k) cleared Class II cryosurgical tool indicated for the destruction of unwanted tissue during surgical procedures, including in adults with chronic rhinitis.
Bethlehem ENT, Bethlehem
Tracy Byerly, MD, Fredericksburg
San Francisco Otolaryngology Medical Group, San Francisco
Arrinex, Inc.
INDUSTRY