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Abbott Initiates U.S. Study of Absolute Pro(TM) Peripheral Stent System for Iliac Artery Disease
Date:4/1/2009

ny's commitment to researching and developing advanced products in both the endovascular and coronary areas to improve patients' overall vascular care."

Abbott's robust vascular research program includes clinical trials in peripheral artery disease, carotid artery disease, and coronary artery disease. Key products in the vascular pipeline include: the Omnilink Elite(TM) Peripheral Stent System; the EMBOSHIELD NAV6(TM) Embolic Protection System for carotid stenting; a fully bioabsorbable drug eluting coronary device; and the XIENCE PRIME(TM) Everolimus Eluting Coronary Stent System, which builds on the proven performance of Abbott's market-leading XIENCE V(R) Everolimus Eluting Coronary Stent System.

EMBOSHIELD NAV6 is pending 510(k) clearance by the United States Food and Drug Administration (FDA) and is not available for sale. Omnilink Elite, the bioabsorbable drug eluting device, and XIENCE PRIME are in development and are not available for sale.

About the Absolute Pro Peripheral Stent System

Abbott's Absolute Pro peripheral stent is a self-expanding nitinol stent with a flexible and conformable design that is intended to keep lesions open without introducing more metal than necessary to treat a narrowing. The peripheral stent delivery system is compatible with 0.035'' (0.89 mm) guide wires. The Absolute Pro Peripheral Self-Expanding Stent is currently an investigational device in the United States for the treatment of iliac artery disease.

About XIENCE V

Abbott's market-leading XIENCE V drug eluting stent is marketed in the United States, Europe and other international markets. XIENCE V is an investigational device in Japan and is currently under review by Japan's Ministry of Health, Labour and Welfare and the Pharmaceuticals and Medical Devices Agency.

Additional information about XIENCE V, including important safety and effectiv
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SOURCE Abbott
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