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April 28, 2021

Vesalio’s NeVa VS Studied in VITAL Clinical Trial to Support FDA Clearance

April 28, 2021—Vesalio announced the completion of enrollment in the VITAL clinical trial evaluating the company’s NeVa VS in the treatment of symptomatic cerebral vasospasm after aneurysmal subarachnoid hemorrhage.

The study, conducted under an investigational device exemption from the FDA, is intended to support the device’s clearance for the United States neurovascular market.

Vesalio’s NeVa platform was designed to achieve first-pass recanalization in acute ischemic stroke by removing all types of neurovascular clots from patient anatomy, stated the company.

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April 29, 2021

AHA Policy Statement Proposes 20% Reduction in Nontraumatic Lower Extremity Amputation by 2030

April 28, 2021

Study Evaluates the Impact of PERT Consultations on Outcomes During the COVID-19 Pandemic


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