Vascular plugs
MVP
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
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Where to buy MVP
Contact Medtronic, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From medtronic.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
FDA clearances
- 510(k) K150108 April 2015
- 510(k) K141313 June 2014
Procedures that use vascular plugs
Frequently asked questions
What is MVP used for?
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Who makes MVP?
MVP is made by Medtronic, Inc.. It is listed under vascular plugs (amplatzer and micro vascular plugs), embolization coils in our device library.
What sizes does MVP come in?
The FDA device database does not list sizes for MVP. Check the instructions for use or ask a Medtronic, Inc. representative.
Is MVP MRI safe?
The FDA device database lists MVP as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is MVP FDA cleared?
MVP is covered by FDA submissions K141313, K150108.
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.