Abbott’s Esprit BTK System Gains the US FDA’s Approval for Chronic Limb-Threatening Ischemia (CLTI) Below-The-Knee (BTK)

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The US FDA has approved Esprit BTK Everolimus Eluting Resorbable Scaffold System (Esprit BTK System) intended for chronic limb-threatening ischemia (CLTI) below-the-knee (BTK)
The approval was based on the LIFE-BTK study that assessed the Esprit BTK System & depicted reduction in disease progression plus improved clinical outcomes vs balloon angioplasty (current SoC). The results were highlighted at 35th TCT Conference in Oct 2023 & published in The New England Journal of Medicine
The Esprit BTK System is a dissolvable stent that opens the blockage, transfers Everolimus & promotes vessel healing before dissolving. It supports the vessels for ~3yrs. enabling them to stay open independently

Ref: Abbott | Image: Abbott

Related News:- Abbott Reports Trial Results for Esprit BTK in Chronic Limb-Threatening Ischemia (CLTI)

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