Atherectomy

Jetstream Sc

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 Sc models and sizes

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

Model / catalog no.SizeMRIStatus
112260-001— Not statedAvailable
112262-001— Not statedAvailable

Procedures that use atherectomy

Frequently asked questions

What is Jetstream Sc 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 Sc?

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

What sizes does Jetstream Sc come in?

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

Is Jetstream Sc MRI safe?

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

Is Jetstream Sc FDA cleared?

Jetstream Sc 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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