{"id":36980,"date":"2025-07-09T11:42:41","date_gmt":"2025-07-09T03:42:41","guid":{"rendered":"https:\/\/flcube.com\/?p=36980"},"modified":"2025-07-09T11:42:42","modified_gmt":"2025-07-09T03:42:42","slug":"boston-scientifics-farapulse-gains-fda-approval-for-expanded-use-in-persistent-atrial-fibrillation","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=36980","title":{"rendered":"Boston Scientific&#8217;s FARAPULSE Gains FDA Approval for Expanded Use in Persistent Atrial Fibrillation"},"content":{"rendered":"\n<p>US-based Boston Scientific Corporation (<a href=\"https:\/\/www.google.com\/finance\/quote\/BSX:NYSE\">NYSE: BSX<\/a>) announced that it has received US FDA approval for label expansion relating to its FARAPULSE pulsed field ablation (PFA) system. The product can now be used to treat drug-refractory, symptomatic persistent atrial fibrillation (AF), a condition where the heart beats abnormally for at least seven days.<\/p>\n\n\n\n<p><strong>Mechanism and Approval<\/strong><br>The FARAPULSE PFA system delivers pulsed electric field energy via a catheter to ablate heart tissue, thereby treating atrial fibrillation. This expanded approval is primarily supported by clinical evidence from the first phase of the ADVANTAGE AF trial, which met its primary safety and efficacy endpoints.<\/p>\n\n\n\n<p><strong>Clinical Trial Results<\/strong><br>Results from the trial showed that no stroke, pulmonary vein stenosis, atrial-esophageal fistula, or major access complications occurred. The symptomatic AF recurrence-free rate was 85.3%. For operators who have performed three or more procedures, the freedom from persistent AF symptoms after FARAPULSE treatment increased to 91.4%.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>US-based Boston Scientific Corporation (NYSE: BSX) announced that it has received US FDA approval for&#8230;<\/p>\n","protected":false},"author":1,"featured_media":36983,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,22],"tags":[315,1160,15],"class_list":["post-36980","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-medical-device","tag-boston-scientific","tag-nyse-bsx","tag-product-approvals"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.5) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Boston Scientific&#039;s FARAPULSE Gains FDA Approval for Expanded Use in Persistent Atrial Fibrillation - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"US-based Boston Scientific Corporation (NYSE: BSX) announced that it has received US FDA approval for label expansion relating to its FARAPULSE pulsed field ablation (PFA) system. 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