Peripheral stents

Innova Vascular

by Boston Scientific Corporation

A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.

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Innova Vascular models and sizes

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

Model / catalog no.SizeMRIStatus
H74939293050230β€” MR ConditionalAvailable
H74939293050270β€” MR ConditionalAvailable
H74939293051030β€” MR ConditionalAvailable
H74939293051070β€” MR ConditionalAvailable
H74939293051230β€” MR ConditionalAvailable
H74939293051270β€” MR ConditionalAvailable
H74939293051530β€” MR ConditionalAvailable
H74939293051570β€” MR ConditionalAvailable
H74939293051830β€” MR ConditionalAvailable
H74939293051870β€” MR ConditionalAvailable
H74939293052030β€” MR ConditionalAvailable
H74939293052070β€” MR ConditionalAvailable
H74939293054030β€” MR ConditionalAvailable
H74939293054070β€” MR ConditionalAvailable
H74939293056030β€” MR ConditionalAvailable
H74939293056070β€” MR ConditionalAvailable
H74939293058030β€” MR ConditionalAvailable
H74939293058070β€” MR ConditionalAvailable
H74939293060230β€” MR ConditionalAvailable
H74939293060270β€” MR ConditionalAvailable
H74939293061030β€” MR ConditionalAvailable
H74939293061070β€” MR ConditionalAvailable
H74939293061230β€” MR ConditionalAvailable
H74939293061270β€” MR ConditionalAvailable
H74939293061530β€” MR ConditionalAvailable
H74939293061570β€” MR ConditionalAvailable
H74939293061830β€” MR ConditionalAvailable
H74939293061870β€” MR ConditionalAvailable
H74939293062030β€” MR ConditionalAvailable
H74939293062070β€” MR ConditionalAvailable
H74939293064030β€” MR ConditionalAvailable
H74939293064070β€” MR ConditionalAvailable
H74939293066030β€” MR ConditionalAvailable
H74939293066070β€” MR ConditionalAvailable
H74939293068030β€” MR ConditionalAvailable
H74939293068070β€” MR ConditionalAvailable
H74939293070230β€” MR ConditionalAvailable
H74939293070270β€” MR ConditionalAvailable
H74939293071030β€” MR ConditionalAvailable
H74939293071070β€” MR ConditionalAvailable
H74939293071230β€” MR ConditionalAvailable
H74939293071270β€” MR ConditionalAvailable
H74939293071530β€” MR ConditionalAvailable
H74939293071570β€” MR ConditionalAvailable
H74939293071830β€” MR ConditionalAvailable
H74939293071870β€” MR ConditionalAvailable
H74939293072030β€” MR ConditionalAvailable
H74939293072070β€” MR ConditionalAvailable
H74939293074030β€” MR ConditionalAvailable
H74939293074070β€” MR ConditionalAvailable
H74939293076030β€” MR ConditionalAvailable
H74939293076070β€” MR ConditionalAvailable
H74939293078030β€” MR ConditionalAvailable
H74939293078070β€” MR ConditionalAvailable
H74939293080230β€” MR ConditionalAvailable
H74939293080270β€” MR ConditionalAvailable
H74939293081030β€” MR ConditionalAvailable
H74939293081070β€” MR ConditionalAvailable
H74939293081230β€” MR ConditionalAvailable
H74939293081270β€” MR ConditionalAvailable
H74939293081530β€” MR ConditionalAvailable
H74939293081570β€” MR ConditionalAvailable
H74939293081830β€” MR ConditionalAvailable
H74939293081870β€” MR ConditionalAvailable
H74939293082030β€” MR ConditionalAvailable
H74939293082070β€” MR ConditionalAvailable
H74939293084030β€” MR ConditionalAvailable
H74939293084070β€” MR ConditionalAvailable
H74939293086030β€” MR ConditionalAvailable
H74939293086070β€” MR ConditionalAvailable
H74939293088030β€” MR ConditionalAvailable
H74939293088070β€” MR ConditionalAvailable

FDA clearances

  • PMA P140028 September 2016

Procedures that use peripheral stents

Frequently asked questions

What is Innova Vascular used for?

A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.

Who makes Innova Vascular?

Innova Vascular is made by Boston Scientific Corporation. It is listed under peripheral artery stents and covered stents in our device library.

What sizes does Innova Vascular come in?

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

Is Innova Vascular MRI safe?

The FDA device database lists Innova Vascular as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Innova Vascular FDA cleared?

Innova Vascular is covered by FDA submission P140028.

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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