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Abbott Announces FDA Approval of First-of-its-kind Device to Repair Leaky Tricuspid Heart Valve, TriClip

Abbott has announced U.S Food and Drug Administration (FDA) approval of its TriClip, a first-of-its-kind device to repair leaky tricuspid heart valve, for which more than 1.6 million people in the U.S. are estimated to be affected. Data from the TRILUMINATE Pivotal trial demonstrated that patients who received TriClip experienced a marked improvement in the severity of their symptoms and quality of life, with benefits sustained at one year. ....

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Abbott (ABT) Receives FDA Approval for TriClip

Abbott (ABT) Receives FDA Approval for TriClip
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FDA Approves TriClip TEER Device for Tricuspid Repair

The approval was based on positive data from the TRILUMINATE pivotal trial, which included a highly symptomatic population. ....

Paul Sorajja , Circulatory System Devices Panel , Drug Administration , System Devices Panel , Allina Health Minneapolis Heart Institute , Abbott Northwestern Hospital ,