FDA approves Medtronic ’ s drug-coated balloon to treat long superficial femoral artery lesions

The FDA approved Medtronic‘s (NYSE:MDT) In.Pact Admiral drug-coated balloon to treat long superficial femoral artery lesions up to 360mm in patients with peripheral artery disease, the medtech giant touted today. In a 227-patient global trial, participants treated with Medtronic’s drug-device combination therapy had a one-year patency rate of 89.1% and a clinically-driven target revascularization rate of 7.1%. Get the full story at our sister site, Drug Delivery Business News. The post FDA approves Medtronic’s drug-coated balloon to treat long superficial femoral artery lesions appeared first on MassDevice.
Source: Mass Device - Category: Medical Devices Authors: Tags: Clinical Trials Drug-Device Combinations Food & Drug Administration (FDA) Pharmaceuticals Regulatory/Compliance Vascular Wall Street Beat Medtronic Source Type: news