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AtriCure's Coolrail(TM) Linear Ablation Pen Receives FDA 510(k) Clearance
Date:3/18/2008

First Case Performed Using Coolrail(TM) Pen in Combination with AtriCure's

ORLab(TM) System - Expands Minimally Invasive Ablation Procedure

WEST CHESTER, Ohio, March 18 /PRNewswire-FirstCall/ -- AtriCure, Inc. (Nasdaq: ATRC), a medical device company and leader in cardiac surgical ablation systems, today announced that its Coolrail(TM) linear ablation pen received 510(k) clearance from the FDA for the ablation of cardiac tissue. Additionally, the first patient was successfully treated using the AtriCure Coolrail(TM) Linear Ablation Pen. The Coolrail(TM) linear ablation pen and ORLab(TM) system were used during a procedure performed by Dr. James R. Edgerton, a prominent cardiac surgeon from the Cardiopulmonary Research Science and Technology Institute of Dallas, Texas. The Coolrail(TM) linear ablation pen is designed to facilitate the creation of an expanded cardiac ablation lesion set during a minimally invasive off-pump procedure. The ORLab(TM) system is a mapping, recording and stimulating system which enables electrophysiologists and surgeons to confirm, in the operating room, that the cardiac ablation lines being created are forming electrical barriers, or lines of conduction block. The protocol used for mapping with the ORLab(TM) system was developed by Dr. Warren M. Jackman, a prominent electrophysiologist.

Dr. James R. Edgerton commented, "We are encouraged by the results of the combined use of AtriCure's Coolrail(TM) pen and ORLab(TM) system to more effectively perform an expanded cardiac ablation procedure. Based on our previous research, we anticipate that our investigation of these new products will demonstrate improved results in patients with persistent and long- standing persistent atrial fibrillation." Dr
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SOURCE AtriCure, Inc.
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