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CryoCor Invited to Participate in FDA Advisory Panel Meeting on Atrial Fibrillation
Date:9/11/2007

SAN DIEGO, Sept. 11 /PRNewswire-FirstCall/ -- CryoCor, Inc. (Nasdaq: CRYO), a medical device company focused on the treatment of cardiac arrhythmias, announced today that it has been invited to participate in a Food and Drug Administration (FDA) panel meeting to be held on September 20, 2007 from 8:00 am to 6:00 pm ET in Gaithersburg, Maryland. The FDA panel committee will discuss and make recommendations regarding clinical trial designs for cardiac ablation devices designed to treat patients with medically refractory atrial fibrillation.

Helen Barold, M.D., Chief Medical Officer of CryoCor, said, "We look forward to adding our experience to this general panel discussion on clinical trials for atrial fibrillation ablation."

About CryoCor

CryoCor is a medical technology company that has developed and manufactures a disposable catheter system based on its proprietary cryoablation technology for the minimally invasive treatment of cardiac arrhythmias. The Company's product, the CryoCor Cardiac Cryoablation System, or the Cryoablation System, is designed to treat cardiac arrhythmias through the use of cryoenergy, or extreme cold, to destroy targeted cardiac tissue. The Cryoablation System has been approved in Europe for the treatment of atrial fibrillation, and atrial flutter, the two most common and difficult to treat arrhythmias, since 2002. In the United States, CryoCor is conducting a pivotal trial to evaluate the safety and efficacy of the Cryoablation System for the treatment of atrial fibrillation and the Cryoablation System has been approved for the treatment of right atrial flutter. For more information please visit the Company's website at http://www.cryocor.com.

Forward Looking Statements

The statements in this press release that are not descriptions of historical facts are forward-looking statements that are subject to risks and uncertainties. The actual events or results
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SOURCE CryoCor, Inc.
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