Gore & Associates announced FDA approval of an expanded indication for the company’s Viabahn VBX balloon expandable e ...
FEVAR and BEVAR transformed how complex aortic aneurysms are treated. Clinicians now have an FDA-approved bridging stent option specifically indicated for these procedures.
W. L. Gore & Associates' medical business (Gore) today announced U.S. Food and Drug Administration approval of an expanded indication for the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (VBX ...
The balloon-expandable device can now be used as a bridge in fenestrated and branched endovascular aortic repair.
Gore today announced US Food and Drug Administration (FDA) approval of an expanded indication for the company's Viabahn VBX ...
The expanded indication covers the device’s use as a bridging stent in fenestrated and branched aortic repair.
(Bild: Redaktion Devicemed; KI-generiertes Symbolbild) Die FDA hat die Zweckbestimmung des ballonexpandierbaren ...
The Advanced Research Projects Agency for Health (ARPA-H) has awarded Siemens Healthineers up to $31.1 million over five years to accelerate the development of autonomous, remote, endovascular ...