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MicroVention Announces First Trial Enrollment In Their U.S. Clinical Trial Of Its New Dual-Layer Stent For Cerebral Aneurysm Flow Diversion
Date:7/22/2013

rovide patients with improved treatment options."

Richard Cappetta, President and CEO of MicroVention, Inc. noted that, "The FRED™ system study is intended to provide clinical evidence that MicroVention's next-generation flow diverter device can effectively treat these difficult aneurysms, and offer new endovascular treatment options for physicians. The enhanced visibility and ease of delivery and deployment, key features of the FRED™ system device, will hopefully result in improved clinical outcomes."

A description of this clinical trial can be found at http://clinicaltrials.gov; Study Number: NCT01801007, as required by U.S. Law.

About the FRED™ system
The Flow Re-Direction Endoluminal Device (FRED) system is the next generation flow diversion device intended for the treatment of intracranial aneurysms.  The FRED™ system is an innovative, uniquely paired, integrated dual-layer (stent-within-a-stent) self-expanding nitinol braided design, which is simultaneously deployed by a single operator through a .027 (0.69 mm) inner diameter Headway™ 27 microcatheter.  The higher radial force outer stent, along with the low porosity-high metal surface area inner stent, unite to provide superb ease of use, enhanced stent opening, improved vessel apposition and fluoroscopic visibility, to help reduce and redirect blood flow into the aneurysm sac.  The FRED™ system offers additional benefits over first generation flow diversion devices, by its ability to be partially deployed, retrieved and accurately repositioned/redeployed, without the need for a torque device. 

About MicroVention, Inc.
MicroVention, Inc. is a U.S. subsidiary of Terumo Corporation with its corporate headquarters in Tustin, California, and manufacturing and administrative facilities in Santa Ana'/>"/>

SOURCE MicroVention, Inc.
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