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AGA Medical Corporation Receives CE Mark Approval for the AMPLATZER(R) Vascular Plug III
AGA Medical Corporation Receives CE Mark Approval for the AMPLATZER(R) Vascular Plug III
MINNEAPOLIS, May 15 /PRNewswire/ -- AGA Medical Corporation ("AGA")
announced today it received CE mark approval to market the AMPLATZER(R)
Vascular Plug III ("AVP III"). AGA also announced the immediate availability
and launch of the device in the European Union. The AVP III further expands
the AGA family of occlusion devices designed to embolize, or close, blood
vessels and blood vessel malformations in the peripheral vasculature.
"We believe the new AVP III is another strong addition to the AGA vascular
plug family," said Franck Gougeon, President and CEO of AGA. "Our goal is to
provide physicians with a toolbox of embolization devices that can treat
vessels of different types and length and with different flow
characteristics."
The AVP III is a self-expanding nitinol mesh device and is designed to be
introduced in a minimally invasive fashion through a catheter. The device
comes pre-attached to a delivery cable by a small screw; the delivery cable
enables the physician to precisely position the device in the targeted blood
vessel. Once positioned, the cable is unscrewed and the device is released.
The nitinol mesh retention discs ensure the secure positioning of the device
even in high flow vessels.
"Our pre-clinical testing suggests that the AVP III will have the fastest
occlusion times within our vascular plug family," said Mr. Gougeon.
The AVP III is under review by the Food and Drug Administration for
clearance to market in the U.S.
ABOUT AGA MEDICAL: AGA Medical Corporation, based inPlymouth, Minnesota
(just outsideMinneapolis), is a leader in developing interventional devices
to treat structural heart defects. As a result of the many contributions and
creative genius of Dr. Kurt Amplatz, AGA develops and commercializes a series
of devices that have revolutionized the treatment of the most common
congenital "holes in the heart" such as atrial septal and patent foramen ovale
defects. The company is expanding into new areas such as the minimally
invasive repair of vascular abnormalities. More than 770 articles have been
published in medical publications that support the benefits of AGA devices,
including improved patient outcomes, reduced length of stay and accelerated
recovery times for the patient. AGA Medical devices have received regulatory
approval and are marketed in 101 countries with more than 278,000 devices
shipped to date. For more information visit www.amplatzer.com.
MEDIA CONTACT:
Jake Sargent
Brunswick Group LLC
202.393.7337
jsargent@brunswickgroup.com
SOURCE AGA Medical Corporation
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Copyright © 2008, NewsBlaze,
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Tags: Healthcare, Pharmaceuticals, Health, minnesota
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