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Home » FDA approves Medtronic’s In.Pact 018 drug-coated balloon catheter

FDA approves Medtronic’s In.Pact 018 drug-coated balloon catheter

May 31, 2022 By Sean Whooley

Medtronic In.Pact 018 drug-coated balloon catheter
Medtronic’s In.Pact 018 DCB. [Image from Medtronic]
Medtronic (NYSE:MDT) announced that it received FDA approval for its In.Pact 018 paclitaxel-coated balloon catheter.

Fridley, Minnesota–based Medtronic’s In.Pact 018 paclitaxel-coated percutaneous transluminal angioplasty (PTA) balloon catheter, a drug-coated balloon product, received an indication for the interventional treatment of peripheral arterial disease (PAD) in the superficial femoral and popliteal arteries.

According to a news release, In.Pact 018 uses the same drug coating formulation as — and was built upon equivalent technology to — the In.Pact Admiral DCB. The In.Pact 018 will be used for PTA of de novo, restenotic or in-stent restenotic lesions with lengths up to 360 mm with vessel diameters of 4-7 mm.

Get the full story at our sister site, Drug Delivery Business News.

Filed Under: Cardiovascular, Catheters, Drug-Device Combinations, Featured, News Well, Pre-Market Approval (PMA), Regulatory/Compliance, Vascular

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About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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