Melody(R) Transcatheter Valve Demonstrates Encouraging Results in Study on Patients with Congenital Heart Disease

The first-of-its kind device is currently under review by the U.S. Food and Drug Administration (FDA) for approval of a humanitarian device exemption (HDE), based on evidence of safety and probable benefit for the Melody valve. On July 22, an FDA advisory panel voted unanimously to recommend conditional approval of the Melody valve, but the device remains investigational in the United States until FDA makes a final decision.

"The Melody transcatheter valve is a viable procedural alternative designed to reduce the number of invasive surgeries and their associated risks," said Dr. Evan Zahn, director of cardiology at Miami Children's Hospital's Congenital Heart Institute and lead author of the published study. "It represents an exciting breakthrough for individuals who typically require numerous open-heart surgeries during the course of their lifetime."

The study is the first prospective, multi-center trial conducted to evaluate the implantation of the Melody valve. The JACC article reports procedural success in 97 percent of patients; encouraging immediate and six-month patient outcomes with improvements in heart and valve function; and overall acceptable study safety outcomes with no deaths or long-term procedure-related medical complications.

"Our goal is to provide effective treatment options for patients with congenital heart disease, and the Melody Pulmonary Transcatheter Valve is an important part of our strategy to develop and deliver transcatheter therapies for diseased valves in all positions of the heart," said Dr. John Liddicoat, vice president and general manager of the Structural Heart division, part of the CardioVascular business at Medtronic. "We are very pleased with the ongoing clinical results of the Melody valve and look forward to bringing this exciting therapy to patients in the United States."

The Melody valve is the first transcatheter valve of any kind to be approved for use anywhere in the world, having received regulatory approvals in Western Europe and Canada in 2006. To date, more than 1,000 patients worldwide have benefited from the Melody valve.

The pulmonary valve connects the heart to the lungs, where blood is enriched with oxygen before being pumped to the rest of the body. About 34,000 infants are born with congenital heart disease every year in the United States. A small percentage of these patients are born with a malformation of the blood flow path between the right side of the heart and the lungs. Early in life, these patients must undergo open-heart surgery to implant a prosthetic valved-conduit to establish adequate blood flow. Medtronic is providing more options for these congenital heart disease patients, who often require multiple open heart surgeries throughout their lifetime to maintain their implanted conduit.

Medtronic CardioVascular is committed to advancing the treatment of coronary, peripheral, aortic and structural heart disease through innovation and collaboration with leading clinicians, researchers and scientists worldwide.

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Medtronic, Inc. (www.medtronic.com), headquartered in Minneapolis, is the global leader in medical technology -- alleviating pain, restoring health and extending life for millions of people around the world.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's Annual Report on Form 10-K for the year ended April 24, 2009. Actual results may differ materially from anticipated results.

SOURCE: Medtronic, Inc.

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