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This is really the first valve that can be delivered via catheter where previously open-heartsurgery was the only option for patients healthy enough to undergo the procedure,” said Brian O’Neill, M.D. director of Interventional and Structural Heart Research at Henry Ford Hospital. William O’Neill, M.D.
Food and Drug Administration ( FDA ) granted an Investigational Device Exemption (IDE) to initiate a US Pivotal Study with its technology. Over 100 patients have been treated with the HighLife technology within different clinical programs in the USA, Europe and APAC. Javits Convention Center, North.
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In addition, the Center has been able to withstand the widely perceived “brain drain” in other sectors, through ensuring opportunities for surgeons to academically advance, conduct research, integrate new technology in practice, and sustain international collaborations.
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