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This is a Food and Drug Administration (FDA) designated Investigational Device Exemption (IDE # G0902212) US Pivotal Trial of a portable pneumatic driver (PPD) for the Total Artificial Heart (TAH). The study is funded by the manufacturer of the TAH and PPD (Syncardia, Inc Tuczon, Az). The Study data will be fully reviewed and adjudicated November 30, 2012 and will be available for the full abstract...
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