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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Aug. 20, 2019

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V-Wave wins breakthrough designation from the FDA for its heart failure device

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Study revives debate over CT perfusion for the coronary arteries

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Vanderbilt researchers weaponize white blood cells to track and kill cancer cells

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Indian government sets up MDTAG to advise regulators on med tech

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Regulatory front

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Financings

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Appointments and advancements

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Daily M&A

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Other news to note

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Product clinical data for Aug. 19, 2019

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Product regulatory actions for Aug. 19, 2019

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BioWorld MedTech's Cardiology Extra

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Cvrx clinches FDA approval for Barostim Neo heart failure device

The FDA has granted its final approval to the first neurostimulation device designed to treat the symptoms of heart failure. Cvrx Inc.'s Barostim Neo system received premarket approval on Friday for the improvement of symptoms in patients with advanced heart failure who are not eligible for treatment with cardiac resynchronization therapy or other heart failure devices. Read More

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