CryoLife Announces SEC Investigation
This investigation is a non-public, fact-finding inquiry. We are trying
to determine whether there have been any violations of the federal
securities laws. The investigation and the subpoena do not mean that we
have concluded that anyone has broken the law. Also the investigation
does not mean that we have a negative opinion of any person, entity or
security.
CryoLife President and CEO, Steven G. Anderson stated that the Company would
cooperate fully with the SEC's investigation.
Founded in 1984, CryoLife, Inc. is the leader in the development and commercialization of implantable living human tissues for use in surgeries throughout the United States and Canada. The Company's BioGlue(R) surgical adhesive is FDA approved as an adjunct to sutures and staples for use in adult patients in open surgical repair of large vessels and is CE marked in the European Community and approved in Canada and Australia for use in vascular and pulmonary sealing and repair. The Company also manufactures the SynerGraft(R) heart valve and the SynerGraft vascular graft, the world's first tissue-engineered heart valve and vascular replacement, respectively, and the CryoLife-O'Brien(R) and CryoLife-Ross(R) stentless porcine heart valves, which are CE marked for distribution within the European Community.
For additional information about the company, visit CryoLife's web site: http://www.cryolife.com .
Contact: D. Ashley Lee
Vice President, Chief Financial Officer
(800) 438-8285
