January 24, 2014 — The U.S. Food and Drug Administration (FDA) cleared Radius Medical LLC’s Prodigy Support Catheter. Engineered to provide back-up support to guidewires, the Prodigy Support Catheter is intended for use in treating chronic total occlusions (CTOs).
Technology | January 24, 2014
FDA Clears Radius Medical’s Prodigy Support Catheter
The Prodigy Support Catheter is designed to stabilize catheters within vessels for enhanced guidewire pushability. The device includes an elastomeric balloon to allow for anchoring of the catheter within the vessel. The balloon material allows for a single balloon to cover vessel diameters from 2 to 6 mm.
"The beauty of this 5 French catheter system is that it's compatible with all conventional guiding catheters and its enhanced trackability through tortuous coronary anatomies," said Richard Heuser, M.D., chief of cardiology, St. Luke's Medical Center, Phoenix, Ariz. "What is so remarkable about this device is its soft, atraumatic balloon that provides protection against damage to the vessel wall, especially in critical cases."
For more information: www.radiusmed.com