The LOTUS Edge valve system is the only FDA-approved aortic valve that gives physicians the option to reposition and completely recapture the valve once it has been fully deployed. It also features a braided valve frame and an adaptive seal that minimizes paravalvular regurgitation or leaking (PVL) by conforming to the patient's native aortic valve.
"We finally received the feedback from G-MED on the IRRAflow after a lengthy period," said Kleanthis G. Xanthopoulos, Ph.D, President and CEO of IRRAS.
The DEEP IDE trial is intended to establish the safety and effectiveness of a dual epicardial and endocardial ablation procedure for patients with persistent or long-standing persistent atrial fibrillation
The purpose of Synaptive’s Evry, a dedicated head MRI, is specifically for imaging patients in situations that require immediate decision making, such as with acute stroke.