Heart Bypass Surgery
Cardica Receives 510(k) Clearance for C-Port Flex a System for Use in Coronary Artery Bypass Surgery
Published in Healthcare Finance, Tax and Law Weekly, April 18th, 2007
Cardica, Inc. (NASDAQ:CRDC) announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its C-Port Flex A Anastomosis System in the United States. The Flex A is a variation of Cardica's C-Port(R) xA Distal Anastomosis System product line and further facilitates the automated anastomosis, or attachment of blood vessels and grafts, during less invasive coronary artery bypass graft (CABG) procedures.
"This is an important milestone for Cardica and a potential break-through advancement for the field of cardiothoracic surgery, as the Flex A system may enable surgeons to perform less invasive bypass surgeries while maintaining...
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