FDA Clears Radius Medical’s Prodigy Support Catheter

 

January 24, 2014
Radius Medical Prodigy Support Catheter Guidewire Cath Lab Elastomeric Balloon

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).

 
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 
The content of this field is kept private and will not be shown publicly.
Type the characters you see in this picture. (verify using audio)
Type the characters you see in the picture above; if you can't read them, submit the form and a new image will be generated. Not case sensitive.