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First Patient Enrolled in Lutonix Drug-Coated Balloon Pivotal Trial
Date:7/25/2011

s up the artery to restore blood flow, and delivers the drug to the artery wall.  The Moxy balloon is then removed from the body leaving nothing behind but the drug coating, which works inside the artery over time to prevent restenosis.  The Moxy balloon is an investigational device, which is not approved for, or available for sale in, the United States.

About Restenosis

Restenosis refers to the re-narrowing of an artery following angioplasty or stenting.  Restenosis is caused by an overgrowth of tissue inside the artery, typically in response to injury caused at the original treatment site.  Restenosis often occurs within the first 6 months following an intervention, and most often results in re-treatment.

About Lutonix, Inc. (www.lutonix.com)

Lutonix is a venture-backed medical device company based in Minneapolis, MN.   The company is dedicated to the development and commercialization of a safe, efficacious drug-coated balloon for the treatment of coronary and peripheral vascular disease.   Current investors include Delphi Ventures, RiverVest Ventures, US Venture Partners, Versant Ventures, Warburg Pincus and The Vertical Group.


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SOURCE Lutonix, Inc.
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