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FDA Panel To Review Atritech’s Watchman Stroke-Prevention Device

This article was originally published in The Gray Sheet

Executive Summary

FDA's Circulatory System Devices panel will meet April 23 to review a PMA for Atritech's Watchman minimally invasive stroke-prevention device for patients with atrial fibrillation, according to the company
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Panel Endorses Atritech Watchman Stroke-Prevention Device In Close Vote

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