SINEXUS SINUS STENT GEN 2, MODEL 1999-25

SINEXUS SINUS STENT GEN 2, MODEL 1999-25 is an FDA 510(k)-cleared medical device (K092401) manufactured by Sinexus, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 16, 2009. Regulation: 8.