Embolic protection
Mo.ma Ultra
An assembly of devices intended to provide cerebrovascular embolic protection during carotid artery angioplasty and stenting procedures. It is available in various configurations and typically includes a sheath/catheter(s), intravascular balloon(s), guidewire, and extracorporeal valves/filters. The assembly is introduced into an artery percutaneously and used to produce blockage of blood through balloon inflation, typically at the carotid bifurcation and internal carotid artery to prevent distal embolization by particulate debris/thrombus and allow removal of debris/thrombus by blood filtration or aspiration. This is a single-use device.
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Where to buy Mo.ma Ultra
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) K092177 October 2009
Procedures that use embolic protection
Frequently asked questions
What is Mo.ma Ultra used for?
An assembly of devices intended to provide cerebrovascular embolic protection during carotid artery angioplasty and stenting procedures. It is available in various configurations and typically includes a sheath/catheter(s), intravascular balloon(s), guidewire, and extracorporeal valves/filters. The assembly is introduced into an artery percutaneously and used to produce blockage of blood through balloon inflation, typically at the carotid bifurcation and internal carotid artery to prevent distal embolization by particulate debris/thrombus and allow removal of debris/thrombus by blood filtration or aspiration. This is a single-use device.
Who makes Mo.ma Ultra?
Mo.ma Ultra is made by Medtronic, Inc.. It is listed under embolic protection devices in our device library.
What sizes does Mo.ma Ultra come in?
The FDA device database does not list sizes for Mo.ma Ultra. Check the instructions for use or ask a Medtronic, Inc. representative.
Is Mo.ma Ultra MRI safe?
The FDA device database entry for Mo.ma Ultra does not state its MRI safety status. Check the labeling before MRI.
Is Mo.ma Ultra FDA cleared?
Mo.ma Ultra is covered by FDA submission K092177.
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.