LUTONIX® Global Real-World Registry 24-Month Outcomes Presented at VIVA 2016

MURRAY HILL, N.J.--(BUSINESS WIRE)--C. R. Bard, Inc. (NYSE:BCR) announced the presentation of the final 24-month results from the LUTONIX® Global Real-World Registry at the Vascular Intervention Advances (VIVA) 2016 Meeting. These results are the first reported final 24-month outcomes for “real-word” registry data for Drug Coated Balloon PTA Catheters (DCBs). The registry includes a subgroup of patients with long femoropopliteal lesions (>140mm) treated with the LUTONIX® 035 DCB. A Premarket Approval Supplement for use in this subgroup population is currently under review with the U.S. Food and Drug Administration.