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With further study, [41] the FDA approved the use of the Taxus stent in the United States in March 2004. [ 42 ] By the end of 2004, drug-eluting stents were used in nearly 80 percent of all percutaneous coronary interventions.
The FDA has given Medtronic approval to use longer lengths of the company's Resolute Integrity drug-eluting stent in treating diabetes patients with coronary artery disease who have long coronary ...
With Johnson & Johnson behind it, and with an additional $100 million invested in its development, the Palmaz stent was approved for use in peripheral arteries in 1991, followed by approval for use in coronary arteries in 1994; Johnson & Johnson quickly captured 90 percent of the market for stents and bought the patent outright from Palmaz ...
The catheter/stent system is introduced into the body by penetrating a peripheral artery (an artery located in the arm or leg) and passed through the arterial system to deliver the DES into the blocked coronary artery. The stent is then expanded to dilate (open) blocked or narrowed coronary arteries (narrowed by plaque buildup), caused by a ...
A drug-eluting stent (DES) is a small mesh tube that is placed in the arteries to keep them open in the treatment of vascular disease.The stent slowly releases a drug to block cell proliferation (a biological process of cell growth and division), thus preventing the arterial narrowing that can occur after stent implantation.
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