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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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