Atherectomy

Jetstream Xc

by Boston Scientific Corporation

A sterile, flexible tube (catheter) intended to be percutaneously introduced for the intraluminal mechanical disruption of atheroma plaque from the walls of peripheral arteries. It has a power-driven cutting or abrasive head for slicing/grinding the atheroma into fragments small enough to be aspirated or absorbed. This device is not intended for use in the coronary, carotid, iliac or renal vasculature. This is a single-use device.

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Jetstream Xc models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
112264-001— Not statedAvailable
112266-001— Not statedAvailable

Procedures that use atherectomy

Frequently asked questions

What is Jetstream Xc used for?

A sterile, flexible tube (catheter) intended to be percutaneously introduced for the intraluminal mechanical disruption of atheroma plaque from the walls of peripheral arteries. It has a power-driven cutting or abrasive head for slicing/grinding the atheroma into fragments small enough to be aspirated or absorbed. This device is not intended for use in the coronary, carotid, iliac or renal vasculature. This is a single-use device.

Who makes Jetstream Xc?

Jetstream Xc is made by Boston Scientific Corporation. It is listed under atherectomy devices in our device library.

What sizes does Jetstream Xc come in?

The FDA device database does not list sizes for Jetstream Xc. Check the instructions for use or ask a Boston Scientific Corporation representative.

Is Jetstream Xc MRI safe?

The FDA device database entry for Jetstream Xc does not state its MRI safety status. Check the labeling before MRI.

Is Jetstream Xc FDA cleared?

Jetstream Xc is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Boston Scientific Corporation sales representative?

Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation 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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