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Medtronic says Evolut TAVR outperformed Edwards Sapien in trial

Medtronic Announces FDA Approval of Newest-generation Evolut TAVR System for Treatment of Symptomatic Severe Aortic Stenosis

The Evolut FX+ TAVR system leverages market-leading valve performance with addition of larger windows to facilitate coronary access

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Medtronic (MDT) Receives FDA Approval of Next-gen Evolut TAVR System

Medtronic (MDT) Receives FDA Approval of Next-gen Evolut TAVR System
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Medtronic announces FDA approval of newest-generation Evolut TAVR system for treatment of symptomatic severe aortic stenosis

Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced that the United States Food and Drug Administration (FDA) has approved the Evolut™ FX+ transcatheter aortic valve replacement (TAVR) system for the treatment of symptomatic severe aortic stenosis. The latest Evolut FX+ TAVR system maintains the valve performance benefits of the legacy Evolut TAVR platform and is designed to facilitate coronary access.

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Medtronic nets FDA approval for evolved Evolut TAVR valve

Medtronic nets FDA approval for evolved Evolut TAVR valve
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