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Argon Announced That The Company Has Received Clearance From Food and Drug Administration

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Core prompt: Argon Medical Devices, Inc. announced today that the company has received clearance from the US Food and Drug Administration to begin marketing the Option™ELITE retrievable inferior ve

Argon Medical Devices, Inc. announced today that the company has received clearance from the US Food and Drug Administration to begin marketing the Option™ELITE retrievable inferior vena cava (IVC) filter with a new over-the-wire delivery technique. This new clearance enables physicians to safely deliver the filter to a patient's IVC by following the path of a guidewire. The guidewire assists in keeping the filter centered in the IVC upon placement.  The over-the-wire technique is a standard of care in many endovascular procedures and the OptionELITE is the only retrievable IVC filter that can be delivered by passing the filter's apex over a guidewire.

"Applying the over-the-wire technique to deliver an IVC filter is a significant development, employing a technique we frequently use during endovascular procedures. It gives a physician more control to accurately position the filter during delivery," said Dr. Munier Nazzal, Chief of Vascular and Endovascular Surgery at the University of Toledo.

Argon is launching the OptionELITE filter with the new over-the-wire delivery technique at the 26th Annual International Symposium of Endovascular Therapy, to be held in Miami Beach, FL from January 18th - 22nd, 2014.  

 
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