Healthcare Industry News: nitinol stent
News Release - November 3, 2010
IDEV Technologies Announces FDA 510(k) Clearance for SUPERA VERITASNew SUPERAŽ Delivery System Improves Procedure Predictability and Stent Performance
WEBSTER, Texas, Nov. 3, 2010 -- (Healthcare Sales & Marketing Network) -- IDEV Technologies, Incorporated (IDEV), an innovative leader in the development and commercialization of minimally invasive medical technologies, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance to market the SUPERA VERITAS Transhepatic Biliary System.
"Clearance of the SUPERA VERITAS system represents the culmination of a strong effort to respond to customer needs," explained Christopher M. Owens, President and CEO of IDEV. "The result is an innovative system that we believe provides us with a significant competitive advantage, and may represent a paradigm shift in how patients are treated."
The new device provides easier deployment of the Supera stent compared to earlier systems, eliminating multiple steps previously required for preparation and delivery. More importantly, the new system allows operators to place the stent more precisely than before.
"I've been deploying the SUPERA stent now for over a year. The high radial force of the stent is particularly suited for biliary strictures. The introduction of the SUPERA VERITAS system is a great complement to an outstanding stent," stated Mark Garcia, MD, Chief of Interventional Radiology at Christiana Care Health System in Wilmington, Delaware.
Gino Sedillo, MD, FACC of Bradenton Cardiology Center in Bradenton, Florida, is an investigator in the SFA trial. He commented, "I've seen the SUPERA VERITAS system demonstrated, and was able to use it myself during a visit to Park Hospital in Leipzig, Germany. The delivery steps have not only been greatly simplified, but there is also improved reliability and predictability of stent placement. I look forward to incorporating the new delivery system into the ongoing prospective trial."
Don Jacobs, MD, a vascular surgeon at St. Louis University Hospital in St. Louis, Missouri, was asked to provide feedback on the new delivery system while in Leipzig, Germany and stated, "I was very impressed with the accuracy of the VERITAS system, and appreciated how it improved the ease of delivery of the SUPERA stent. It represents a truly significant advance and adds significantly to an outstanding product package."
Commercial availability of the SUPERA VERITAS Transhepatic Biliary System is planned for the first quarter of 2011.
About IDEV Technologies, Incorporated
IDEV Technologies, Incorporated (IDEV) is an innovator and developer of next generation medical devices for use in interventional radiology, vascular surgery and cardiology. IDEV's worldwide headquarters is located in Webster, Texas and its European headquarters is located in Beuningen, The Netherlands. Please visit www.idevmd.com.
The SUPERA stent is currently indicated in the U.S. for the palliative treatment of biliary strictures produced by malignant neoplasms and in Europe for the treatment of biliary strictures produced by malignant neoplasms and for peripheral vascular use following failed percutaneous transluminal angioplasty (PTA).
Source: IDEV Technologies
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