510(k) K152121

NuVent EM Sinus Dilation System by Medtronic Xomed, Inc. — Product Code LRC

K152121 is an FDA 510(k) premarket notification submitted by Medtronic Xomed, Inc. for the device "NuVent EM Sinus Dilation System". The FDA issued a decision of Substantially Equivalent on December 1, 2015. The device falls under product code LRC (Instrument, Ent Manual Surgical), a Class I device regulated under 21 CFR 874.4420. Medtronic Xomed, Inc. has at least 10 other 510(k) clearances on record.