ENTELLUS MEDICAL SINUS GUIDEWIRE

ENTELLUS MEDICAL SINUS GUIDEWIRE is an FDA 510(k)-cleared medical device (K110739) manufactured by Entellus Medical, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 13, 2011. Regulation: 8.