In patients with vegetative endocarditis related to cardiac implantable electronic devices (CIEDs), extracting the lead along with percutaneous mechanical debulking via vacuum aspiration of ...
COLORADO SPRINGS, Colo., The Spectranetics Corporation today announced U.S. Food and Drug Administration (FDA) Premarket Notification 510(k) submission of the Bridge Occlusion Balloon. Building on the ...
Please provide your email address to receive an email when new articles are posted on . Xcardia Innovation Ltd., following the February FDA 510(k) clearance of its device for cardiac pacemaker and ...
Cardiac lead extraction is safer in high volume centres, according to the largest study of contemporary practice in Europe published today in European Heart Journal. Extraction in a low volume centre ...
This content is provided by MedStar Washington Hospital Center. Surgically implanted cardiac devices are quite common with more than one million cardiac pacemakers implanted every year worldwide – ...