AngioScore, Inc. Launches New Longer AngioSculpt(R) Devices for Treatment of Peripheral Artery Disease
Published: Apr 01, 2011
The new devices have received U.S. Food and Drug Administration (FDA) 510(k) clearance to market for the dilatation of lesions in the iliac, femoral, ilio-femoral, popliteal, and infra popliteal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. These new PTA catheters are not labeled for use in the coronary or neuro-vasculature.
The new AngioSculpt devices incorporate longer (40 mm) balloons and scoring elements in diameters 2.0, 2.5, 3.0 and 3.5 mm. These new sizes are expected to be particularly useful in treating lesions typically encountered in the treatment of complex PAD below the knee (BTK). Dr. Barry Weinstock, an interventional cardiologist at Orlando Regional Medical Center, commented, “These new longer AngioSculpt devices represent a significant improvement over conventional angioplasty balloons for the treatment of complex lesions because of their ability to achieve more predictable luminal expansion and a lower rate of dissection, thereby minimizing the need to perform adjunctive stenting. This advantage is particularly important when working below the knee as stenting in those vessels is generally undesirable.”
Thomas R. Trotter, president and CEO of AngioScore, added, “The peripheral artery disease market is one of the rapidly growing segments of the overall interventional cardiovascular market worldwide. Over 1.5 million percutaneous peripheral procedures are now being performed annually worldwide, and the growth rate is accelerating due to improved diagnosis and the increasing incidence of important risk factors, such as adult-onset diabetes mellitus. We believe that the AngioSculpt line of Scoring Balloon Catheters is particularly useful in treating this very challenging and serious disease.”
The AngioSculpt Scoring Balloon Catheters represent the next generation in angioplasty balloon catheters for both coronary and peripheral artery disease. Their innovative nitinol scoring elements provide unique circumferential scoring of plaque, leading to precise and predictable luminal enlargement across a wide range of lesion types while avoiding “geographic miss” through their unique anti-slippage properties. The AngioSculpt balloon catheters provide the versatility and effectiveness of a new technology together with the simplicity and deliverability of traditional high-performance balloon catheters.
AngioSculpt devices have now been used in more than 100,000 procedures worldwide and have achieved an outstanding performance record in the treatment of both coronary and peripheral artery disease.
AngioScore, Inc. (www.angioscore.com) is a privately funded endovascular company located in Fremont, California. AngioScore can be contacted at (510) 933-7900 or firstname.lastname@example.org.
Note: This press release contains forward-looking statements that are based upon management’s current expectations and are inherently uncertain. Actual results and timing of events could differ materially from current expectations and forward-looking statements.
AngioScore, Inc. Thomas R. Trotter, CEO 510-933-7914