CryoLife has announced the first European clinical implant of its HeRO (Haemodialysis Reliable Outflow) graft following its CE Mark in June 2013. The procedure was performed at the University of Leuven Hospital in Belgium by Professor ...
Tags: CryoLife, Outflow Graft
CryoLife has received premarket approval from the US Food and Drug Administration (FDA) for its new Sologrip, a minimally invasive laser fiber-optic delivery system. The Sologrip delivery system is a single-use, disposable handset ...
CryoLife, a US-based tissue processing and medical device company, has secured conditional US FDA approval of its Investigational Device Exemption (IDE) for PerClot. A hemostat made of absorbable polysaccharide granules, PerClot is ...
Tags: Cryolife, Trials of Perclot
The US Food and Drug Administration (FDA) has granted 510(k) approval to CryoLife's new Hemodialysis Reliable Outflow (HeRO) device. The device, which the company claims, is the only subcutaneous AV access solution that maintains ...