Drug-coated balloons

In.pact AV

by Medtronic, Inc.

A sterile, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip, and to simultaneously release a drug intended to inhibit restenosis; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single-lumen. This is a single-use device.

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Where to buy In.pact AV

Contact Medtronic, Inc. directly; they can quote, ship, or point you to the distributor for your country.

From medtronic.com, checked October 2026.

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FDA clearances

  • PMA P190008 November 2024

Procedures that use drug-coated balloons

Frequently asked questions

What is In.pact AV used for?

A sterile, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip, and to simultaneously release a drug intended to inhibit restenosis; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single-lumen. This is a single-use device.

Who makes In.pact AV?

In.pact AV is made by Medtronic, Inc.. It is listed under drug-coated balloons in our device library.

What sizes does In.pact AV come in?

Sizes listed for In.pact AV: Length: 40–120 mm; Outer Diameter: 4–12 mm. Confirm availability with the manufacturer's instructions for use.

Is In.pact AV MRI safe?

The FDA device database entry for In.pact AV does not state its MRI safety status. Check the labeling before MRI.

Is In.pact AV FDA cleared?

In.pact AV is covered by FDA submission P190008.

How do I contact a Medtronic, Inc. sales representative?

Medtronic, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic, Inc. company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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