AngioSafe® announced its emergence from stealth with 510(k) clearance from the U.S. FDA for the Santreva™-ATK Endovascular Revascularization Catheter.
This is the second article in a four-part series examining America’s preventable amputation crisis. Read part 1 HERE. “We’re ...
AngioSafe announced it has received FDA 510(k) clearance and CE marking for its Santreva-ATK endovascular revascularization ...
Abbott (NYSE: ABT) today announced that Health Canada has authorized the Esprit™ BTK Everolimus Eluting Resorbable Scaffold ...
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