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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 Esprit™ 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 . ....

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Drug-Eluting Resorbable Scaffold: Hope For Those with Below-knee Vascular Disease

Drug-Eluting Resorbable Scaffold: Hope For Those with Below-knee Vascular Disease
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Everolimus-eluting scaffold found better than angioplasty for CLTI patients with infrapopliteal artery disease

Everolimus-eluting scaffold found better than angioplasty for CLTI patients with infrapopliteal artery disease
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VIVA23 Presents Outcomes of Late-breaking Science from Abbott's LIFE-BTK, RESOLV FIH Study, and IN.PACT AV Access Trial

The second round of late-breaking clinical trials were presented with results from three studies during the Vascular InterVentional Advances Conference, VIVA23, being held Oct. 30-Nov. 2 in Las Vegas, NV. Notably, results from Abbott’s LIFE-BTK randomized clinical trial (RCT) demonstrated that Esprit BTK (Abbott) reduces disease progression and helps improve medical outcomes compared to balloon angioplasty, the current state of care. ....

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Peripheral Circulatory Disease Treatment Market to Exhibit a Remarkable Growth Rate of 7.50% by 2030

Data Bridge Market Research has recently conducted a comprehensive market intelligence study, presenting an in-depth analysis of the Peripheral Circulatory Disease Treatment Market. The freshly published report features an engaging layout that effectively presents crucial data through visually appealing tables, grap. ....

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