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BioWorld - Friday, January 30, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

April 1, 2014

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American College of Cardiology 2014 Meeting: Corevalve wows FDA, will need no advisory for high-risk patients

WASHINGTON — Medtronic (Minneapolis) may have, at least temporarily, moved ahead of rival Edwards Lifesciences (Irvine, California) in the transcatheter aortic valve wars with the announcement that the data are back for the pivotal trial for the CoreValve in high-risk patients. The company announced at this year's annual meeting of the American College of Cardiology (ACC; Washington) that the CoreValve not only yielded better returns on all-cause mortality at a year compared to surgical aortic valve replacement, but also that the device bested surgical valves for stroke at one year, giving the device an edge on the Edwards Sapien in the U.S. market. Read More

Primus jeered for saying Obama 'sympathetic' to tort reform issue

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ACC Notebook: SYMPLICITY HTN-3 details derail renal denervation train

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Nordion to be acquired by Sterigenics for $727 million

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Agreements/contracts: ACell enters purchasing agreement with Novation

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Report from Europe: Sorin receives CE mark for Perceval sutureless valve

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Financings roundup: Stereotaxis amends agreement with Silicon Valley Bank

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Court Report: Baylor Health Care, neurosurgeon face malpractice suit from patient

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People in Places

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MDD's Cardiology Extra

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