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Endovascular Treatment Articles & Analysis

7 news found

Imperative Care Announces First Patient Enrolled in the Imperative Trial Evaluating the Zoom 88 Large Distal Platform for the Treatment of Ischemic Stroke

Imperative Care Announces First Patient Enrolled in the Imperative Trial Evaluating the Zoom 88 Large Distal Platform for the Treatment of Ischemic Stroke

This prospective, multi-center clinical trial is the first study designed to evaluate the clinical benefits of direct aspiration for the treatment of ischemic stroke with the Zoom 88 Large Distal Platform, which is currently FDA cleared for neurovascular access. ...

ByImperative Care


Endologix Launches ALTO™ Abdominal Stent Graft System in Europe

Endologix Launches ALTO™ Abdominal Stent Graft System in Europe

Furthering its mission to transform the treatment of aortic disorders, Endologix LLC today announced the first implant of its ALTO™ Abdominal Stent Graft, commencing the European commercial release of the recently CE Mark approved endograft. ...

ByEndologix LLC


Endologix Announces First Commercial Implant of ALTO Abdominal Stent Graft System Outside of United States

Endologix Announces First Commercial Implant of ALTO Abdominal Stent Graft System Outside of United States

“With the 7 mm infrarenal placement of its sealing ring, ALTO expands the endovascular treatment of AAA patients to include short and challenging aortic necks, which represent a significant portion of the underserved AAA market,” commented Dr. ...

ByEndologix LLC


Endologix Receives CE Mark for ALTO Abdominal Stent Graft System

Endologix Receives CE Mark for ALTO Abdominal Stent Graft System

Transforming the treatment of aortic disorders, Endologix® Inc. (OTC: ELGXQ) (“Endologix” or the “Company”), today announced that it has received a CE Mark for the ALTOTM Abdominal Stent Graft System (ALTO). ...

ByEndologix LLC


Balt Receives IDE Approval From the FDA to Begin the STEM Trial

Balt Receives IDE Approval From the FDA to Begin the STEM Trial

Food and Drug Administration (FDA) to begin The Squid Trial for the Embolization of the Middle meningeal artery (STEM) for the treatment of chronic Sub-Dural Hematoma. Chronic Sub-Dural Hematoma (cSDH) is a common disease affecting primarily older adults. ...

ByBalt USA LLC.


FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

Endospan, a pioneer in off-the-shelf endovascular repair of aortic arch disease was recently granted Breakthrough Device Designation from the U.S. ...

ByEndospan Ltd.


Research Presented at LINC Suggests the Profusa Lumee® Oxygen Platform May Improve Clinical Management of Patients with Critical Limb Ischemia

Research Presented at LINC Suggests the Profusa Lumee® Oxygen Platform May Improve Clinical Management of Patients with Critical Limb Ischemia

Profusa, a digital health company that is pioneering the next generation of personalized medicine, today announced research findings that suggest the company’s Lumee® Oxygen Platform may help improve the clinical management of patients with critical limb ischemia (CLI) who are undergoing endovascular revascularization treatment (EVT). The data, from a ...

ByProfusa, Inc.

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