Press Release:

SynCardia Systems Appoints Michael J. Quinn to Board of Directors

Healthcare Industry Executive to Provide Strategic Guidance
as CardioWest™ temporary Total Artificial Heart Nears FDA Approval

TUCSON, Ariz. – June 16, 2004 – SynCardia Systems, Inc., a privately held developer of biomechanical cardiac replacement and assist devices, today announced the appointment of Michael J. Quinn to its Board of Directors.

Mr. Quinn brings extensive experience and success in leading major healthcare companies to the SynCardia Board. Currently, Mr. Quinn serves as President and Chief Executive Officer of CardioGenesis, the market leader in surgical products and accessories used in angina-relieving Transmyocardial Revascularization (TMR) and Percutaneous Myocardial Revascularization (PMR) procedures. Under his leadership, the company has seen increased sales and heightened demand for its principal products.

Prior to CardioGenesis, Mr. Quinn held a number of executive management positions including Chief Executive Officer, President and Chief Operating Officer at companies including American Hospital Supply Corporation (V. Mueller and Scientific Products Divisions), Picker International, Cardinal Health Group, Bergen Brunswig and Fisher Scientific. He was most recently President and Chief Executive Officer of Premier Laser Systems, a manufacturer of surgical and laser products, and prior to that, he served as President of Imagyn Medical Technologies, a manufacturer of minimally invasive surgical specialty products.

“As SynCardia makes strides toward FDA-approval of the CardioWest™ temporary Total Artificial Heart (TAH-t), we believe Mike’s deep-seeded expertise in the healthcare industry and leadership bringing medical innovations to market will be a great asset to our company,” said Dr. Marvin J. Slepian, president and CEO, SynCardia. “We welcome Mike’s guidance as SynCardia moves from a period of research and development into a period focused on delivering the CardioWest™ TAH-t to the American and European markets.”

“On track to become the first total artificial heart ever approved by the FDA, the CardioWest™ TAH-t is destined to have a powerful and important impact on the healthcare industry,” said Michael Quinn. “I am enthusiastic about the potential of this device and excited to bring my experience to the Board of Directors as SynCardia moves into a new period of growth.”


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About the SynCardia temporary Total Artificial Heart
SynCardia Systems, Inc. (Tucson, AZ) is the privately-held manufacturer of the world's first and only FDA, Health Canada and CE approved Total Artificial Heart. Originally used as a permanent replacement heart, SynCardia's Total Artificial Heart is currently approved as a bridge to transplant for people dying from end-stage biventricular heart failure. There have been more than 950 implants of the Total Artificial Heart, accounting for more than 230 patient years of life.

Similar to a heart transplant, SynCardia's Total Artificial Heart replaces both failing heart ventricles and the four heart valves, eliminating the symptoms and source of end-stage biventricular failure. Unlike a donor heart, the Total Artificial Heart is immediately available at SynCardia Certified Centers and does not require expensive anti-rejection medication, which can cause subsequent complications. It is the only device that provides immediate, safe blood flow of up to 9.5 liters per minute through both ventricles. This high volume of safe blood flow helps speed the recovery of vital organs, helping make the patient a better transplant candidate.

SynCardia Ranked #20 Among World's 50 Most Innovative Companies
In March 2011, Fast Company magazine ranked SynCardia #20 in its annual list of the "World's 50 Most Innovative Companies" for "giving mobility to artificial heart recipients." Weighing 13.5 pounds, SynCardia's Freedom® portable driver is the world's first wearable driver designed to power the Total Artificial Heart both inside and outside the hospital. The Freedom driver is CE approved for use in Europe and undergoing an FDA-approved Investigational Device Exemption (IDE) clinical study in the U.S.

For additional information, please visit: http://www.syncardia.com
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Media Contact:
Don Isaacs
Vice President of Communications
SynCardia Systems, Inc.
Cell: (520) 955-0660

 

 

*The SynCardia temporary Total Artificial Heart was formerly known as the
SynCardia temporary CardioWest™ Total Artificial Heart.

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