Anaconda Biomed, SL, announced that it has received CE Mark certification for its ANA5 advanced neurovascular access funnel ...

Inquis Medical announced that its Aventus mechanical thrombectomy system has received FDA 510(k) clearance for an expanded ...

InspireMD, Inc. recently announced it has received CE Mark approval under the European Medical Device Regulation (EU MDR) for ...

Crossroads Neurovascular, Inc. announced FDA 510(k) clearance for the company’s Path balloon guide catheter (BGC) for neurov ...

TRAINING IN ENDOVASCULAR SURGERY DURING THE MECHANICAL THROMBECTOMY (MT) INNOVATION BOOM. I was fortunate to have completed ...

Penumbra, Inc. announced the completion of enrollment in the pivotal STORM-PE prospective, multicenter, randomized controlled tria ...

The American College of Cardiology (ACC) reported that the Richard A. and Susan F. Smith Center for Outcomes Research at Beth ...

Nectero Medical announced that the American Medical Association’s CPT Editorial Panel has approved two Category III CPT code ...

Medtronic announced the treatment of the first patient in the United States in the Global SYMPLICITY Registry (GSR) DEFINE. The cl ...

Viz.ai announced it has received FDA 510(k) clearance for Viz Subdural Plus, a comprehensive solution for quantifying the ...

A summary of preclinical evaluation methods for neuroendovascular devices, including in vitro techniques, 3D-printed vascular models, in silico simulations, and in vivo models.

Penumbra, Inc. announced that data from the THRIVE study demonstrated the potential of the company’s computer assisted vacuum ...