TriReme Receives FDA Approval for Expanded Matrix of Novel Glider PTCA Balloon Catheter
TriReme Medical, Inc. (TMI) announced today that it has received FDA clearance for an expanded matrix of sizes for its unique Glider™ PTCA balloon catheter. Glider™ is now approved for the treatment of lesions in the coronary vasculature in balloon diameters from 1.5-3.5mm and in lengths from 4mm to 20mm.
"Glider™ provides interventional cardiologists with an entirely new degree of control during the treatment of complex side branches and total occlusions," said Dr. David Rizik, Medical Director and Interventional Cardiologist at Scottsdale Heart Group in Scottsdale, AZ. "With its torqueable shaft and ultra short 4mm length, I am amazed that such a clever design can provide such powerful clinical benefits. Glider™ has become my 'go-to' balloon when I approach the treatment of my most challenging cases."
"Our recent experience in Europe demonstrates Glider's™ ability to outperform conventional 'best in class' balloon catheters," said Eitan Konstantino, president and CEO of TriReme Medical, Inc. "TriReme now has three product families that have received regulatory approval in the United States. I am proud of our development team that continues to bring to market 'out-of-the-box' solutions to simplify complex interventional procedures."