Peripheral stents
Complete Se Vascular
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.
FDA clearances
- PMA P110040 August 2016
- PMA P090006 June 2016
Procedures that use peripheral stents
Frequently asked questions
What is Complete Se 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 Complete Se Vascular?
Complete Se Vascular is made by Medtronic, Inc.. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does Complete Se Vascular come in?
Sizes listed for Complete Se Vascular: Length: 20–150 mm. Confirm availability with the manufacturer's instructions for use.
Is Complete Se Vascular MRI safe?
The FDA device database lists Complete Se Vascular as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Complete Se Vascular FDA cleared?
Complete Se Vascular is covered by FDA submissions P090006, P110040.
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.