Oct 18, 2010 . Medtronic's CoreValve Clinical Trial Receives FDA Approval - Fifteen years ago, endovascular AAA stents were an academic exercise in the .

Oct 19, 2010 . "FDA approval of this groundbreaking clinical trial is a critical step toward a U.S. introduction of CoreValve," said John Liddicoat, M.D., .

Oct 15, 2010 . theflyonthewall.com: Medtronic announces FDA conditional approval for CoreValve. Medtronic announced FDA conditional approval for its .

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4 posts - 3 authors - Last post: Feb 4http://www.theheart.org/article/1174205.do In a move that will no doubt leave investigators sighing with relief, the FDA has granted .

Jan 19, 2011 . FDA lets CoreValve TAVI trial drop medical therapy randomization « Health News: Latest Health Articles, Tips & Advice for Better …

Jan 18, 2011 . approval from the U.S. Food and Drug Administration (FDA) to modify its. CoreValve U.S. Pivotal Clinical Trial. In the revised design, .

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May 17, 2011 . The favorable two-year results from the 18-French CoreValve multicenter . . Aethlon Medical (OTCBB: AEMD) Reports FDA Meeting Request for .

FDA lets CoreValve TAVI trial drop medical therapy randomization. From Preventive Cardiovascular Nurses Association. Remember me on this computer With full .

Medtronic Clinical Trial Receives FDA Approval to Evaluate New CoreValve® System for Aortic Valve Implantation. MINNEAPOLIS -- Medtronic, Inc. announced .

May 28, 2010 . We're actively working with the FDA to bring this therapy to U.S. . or sale of the CoreValve ReValving System in the United States. .

The FDA has allowed Medtronic to modify its CoreValve U.S. pivotal clinical trial. The revised trial will assess the CoreValve system in inoperable patients .

Promising percutaneous CoreValve data from Europe leave US trialists itching .

Mar 17, 2011 . Later in January 2011, Medtronic received conditional approval from FDA to modify its CoreValve US pivotal clinical trial. .

Oct 15, 2010 . Medtronic, Inc. (NYSE: MDT) today announced U.S. Food and Drug Administration ( FDA) conditional approval for its Investigational Device .

Dec 22, 2010 . Landmark Medtronic CoreValve U.S. Clinical Trial Begins. . 4 FDA Approves Home Health App HealthDataManagement, March 4, 2011 .

Oct 13, 2008 . CoreValve (a href http://www.corevalve.com onclick linkClick( t. . is Notified of the FDA Approval of an Additional Magnetic Irrigated .

Feb 11, 2010 . read more. Landmark Medtronic CoreValve® U.S. Clinical Trial Begins2010-12-21 . FDA approves novel heart valve from Medtronic2010-01-25 .

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Jan 20, 2011 . Medtronic receives conditional approval from the US Food and Drug Administration (FDA) to modify its CoreValve US Pivotal Clinical Trial.

FDA Approves Pivotal Trial for Medtronic's CoreValve System. Share · E-mail; Print. October 15, 2010—Medtronic, Inc. (Minneapolis, MN) announced that the US .

Oct 18, 2010 . Fifteen years ago, endovascular AAA stents were an academic exercise in the most progressive vascular surgery departments.

Oct 15, 2010 . Medtronic Clinical Trial Receives FDA Approval to Evaluate New CoreValve® System for Aortic Valve Implantation .

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Jan 18, 2011 . Medtronic Revises Design of CoreValve® U.S. Pivotal Trial . Drug Administration (FDA) to modify its CoreValve U.S. Pivotal Clinical Trial. .

U-M's CoreValve trial to offer less invasive approach for patients with aortic . Medtronic recieves conditional approval from FDA to modify CoreValve U.S. .

Oct 3, 2005 . Medtronic Receives FDA Approval for . CoreValve to Present at Medtech Insight's ``Investment In Innovation'' Conference. .

Medtronic's CoreValve Clinical Trial Receives FDA Approval. by Michael on Oct 18 , 2010 • 11:57 am. No Comments. Fifteen years ago, endovascular AAA stents .

Medtronic's CoreValve Clinical Trial Receives FDA Approval · Email this article to . CoreValve Aortic Valve Replacement System Now With AccuTrak Stability .

Medtronic Clinical Trial Receives FDA Approval To Evaluate New CoreValve(R) System For Aortic Valve Implantation Medtronic, Inc. (NYSE: MDT) today announced .

Oct 15, 2010 . A roundup of recent clinical trial news for medical devices.

Jan 18, 2011 . Medtronic has received conditional approval from the US Food and Drug Administration (FDA) to modify its CoreValve US Pivotal Clinical .

Dec 17, 2010 . Medtronic may have to alter the trial of its CoreValve transcatheter heart . The company is currently in talks with the US FDA about the.

Jan 19, 2011 . January 19, 2011 – The U.S. Food and Drug Administration (FDA) granted conditional approval to modify the CoreValve U.S. pivotal clinical .

Jan 18, 2011. (FDA) to modify its CoreValve U.S. Pivotal Clinical Trial. In the revised design, the trial will assess the CoreValve System in extreme .

FDA lets CoreValve TAVI trial drop medical therapy randomization. January 18, 2011 | Shelley Wood. New York, NY - In a move that will no doubt leave .

Medtronic, Inc. (NYSE: MDT) announced it has received conditional approval from the U.S. Food and Drug Administration (FDA) to modify its CoreValve U.S. .

Jan 18, 2011 . Medtronic Revises Design of CoreValve® U.S. Pivotal Trial . Drug Administration (FDA) to modify its CoreValve U.S. Pivotal Clinical Trial. .

Oct 19, 2010 . New Catheter Aortic Valve Replacement, CoreValve By Medtronic, Gets Approval For FDA Safety & Efficacy Study of Aortic Stenosis Patients.

May 19, 2011 . Medtronic announced Tuesday that its CoreValve System, designed to enable the replacement of a diseased aortic valve without open heart .

CRT unites FDA, industry, physicians—with an eye to Congress . Edwards, CoreValve both claim victory in U.K. heart valve patent suit .

Nov 8, 2005 . The pivotal international clinical trial will use CoreValve's . changes to governmental regulation of medical devices, the FDA's approval .

Jan 19, 2011 . Medtronic Revises Design of CoreValve(R) U.S. Pivotal Trial . Administration ( FDA) to modify its CoreValve U.S. Pivotal Clinical Trial. .

"The CoreValve technology and the ability to perform aortic valve replacement . Centocor Ortho Biotech Inc. Submits Application to FDA Seeking REMICADE .

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Jan 30, 2008 . CoreValve and AccuTrak are not yet available in the United States, Canada or Japan for . Medtronic receives FDA approval for RestoreULTRA .

Mar 17, 2011 . Later in January 2011, Medtronic received conditional approval from FDA to modify its CoreValve US pivotal clinical trial. .

CoreValve Trial Revised, Patients Not Randomized to Medical Therapy January 19, 2011 – The U.S. Food and Drug Administration (FDA) granted conditional .

Apr 2, 2010 . It pertains to an Andersen patent that is currently scheduled to expire before CoreValve products are expected to be approved by the FDA. .

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