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Balloon Angioplasty

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November 12, 2019
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DCB shows durable real-world effectiveness at 4 years

DCB shows durable real-world effectiveness at 4 years

LAS VEGAS — In a real-world population with peripheral artery disease, nearly three-quarters of patients treated with a drug-coated balloon were free from clinically driven target lesion revascularization at 4 years, according to new data presented at VIVA 19.

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November 06, 2019
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RANGER II SFA: Low-dose paclitaxel-coated balloon superior to PTA at 1 year

RANGER II SFA: Low-dose paclitaxel-coated balloon superior to PTA at 1 year

LAS VEGAS — A low-dose paclitaxel-coated balloon was superior to percutaneous transluminal angioplasty for treatment of femoropopliteal disease, according to results from a prespecified interim 1-year analysis from the RANGER II SFA trial presented at VIVA 19.

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September 18, 2019
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Sirolimus-eluting balloon given breakthrough device designation

Sirolimus-eluting balloon given breakthrough device designation

Orchestra BioMed Inc., in partnership with Terumo Corporation, announced its sirolimus-eluting balloon for the treatment of below-the-knee peripheral artery disease, has received breakthrough device designation from the FDA.

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August 02, 2019
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DCB catheter receives FDA breakthrough device designation

B. Braun Interventional Systems announced that a drug-coated balloon catheter for percutaneous transluminal coronary angioplasty has received a breakthrough device designation from the FDA for the treatment of patients with coronary in-stent restenosis.

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