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Established TAVR Platforms Evolving for Lifetime Management

ABBOTT S BREAKTHROUGH DISSOLVING STENT RECEIVES FDA APPROVAL FOR ARTERIES BELOW THE KNEE

Abbott (NYSE: ABT) today announced that the U.S. Food and Drug Administration (FDA) has approved the Espritâ„¢ BTK Everolimus Eluting Resorbable Scaffold System (Esprit BTK System), a breakthrough innovation for people with chronic limb-threatening ischemia (CLTI) below-the-knee (BTK). The Esprit BTK System is .

FDA Approves Abbott s Novel Dissolvable Stent Therapy for Peripheral Artery Disease

FDA approves Abbott s dissolving stent for blocked arteries below the knee

FDA approves Abbott s dissolving stent for blocked arteries below the knee
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FDA approves novel bioresorbable scaffold for treating chronic limb-threatening ischemia

FDA approves novel bioresorbable scaffold for treating chronic limb-threatening ischemia
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