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CryoLife Announces First European Implant Of HeRO Graft
Date:7/31/2013

60; We continue to believe the HeRO Graft represents a significant opportunity to provide a better dialysis access option for patients with end-stage renal disease and that it will be a growth driver for the Company."

About the HeRO Graft

The HeRO Graft received its initial FDA 510(k) clearance in 2008 and initial CE Mark approval in 2011.  It is indicated for catheter dependent ESRD patients on long-term hemodialysis who have exhausted all other access options, such as AV fistulas and grafts (AVFs and AVGs). Prior to the introduction of the HeRO Graft, the only option for these patients was access through percutaneous tunneled dialysis catheters (TDCs), which are higher cost, have high infection rates, limit a patient's lifestyle, and foster central venous stenosis, or narrowing.  The HeRO Graft overcomes the limitations of TDCs by providing a completely subcutaneous graft that functions like a regular access graft during dialysis and provides superior blood flow and a 69 percent reduction in bacteremia (bacteria in the blood) compared with TDCs. HeRO Graft is the only subcutaneous AV access solution clinically proven to maintain long-term access for hemodialysis patients with central venous stenosis.

The HeRO Graft has been implanted in more than 6,000 patients to date and is supported by nearly 130 published clinical studies and presentations.  The product has established reimbursement rates in the U.S., with reimbursement codes that are endorsed by the Society for Vascular Surgery and the American Medical Association.  For more information on the HeRO Graft, visit www.herograft.com.  For additional information about CryoLife, visit the company's Web site: www.cryolife.com.

Statements made in this press release that look forward in time or that express management's beliefs, expectations or hopes are forwa
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SOURCE CryoLife, Inc.
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