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![]() “This acquisition of CoreValve gives additional momentum to our strategies for growth and will improve the quality of care for more than 300,000 people worldwide with severe aortic stenosis,” says Medtronic's CEO and Chairman Bill Hawkins. “Our manufacturing and global distribution strengths will accelerate the use of this life-saving technology.” The ReValving System is a nonsurgical percutaneous aortic valve replacement. It is inserted into a patient through an artery in the groin, as opposed to an invasive, high-risk surgical procedure. The product has been implanted in 2,600 patients at 125 centers in 25 countries, according to CoreValve. The company performed its first in-patient transcatheter valve procedure in 2004, and the ReValving System received CE Mark approval in Europe in 2007. The ReValving System is currently undergoing clinical trials outside of the U.S. It is not available in the U.S. for trials or commercialization. Related headlines 23 Orange County ERs launch health data exchange "OC METRO Minute," Feb. 18: Medtech Insight expects home health care product market to expand "OC METRO Minute," Feb. 11: CHOC Children's participates in bone marrow study OC Family: Pregnancy hormone predicts postpartum depression |
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