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Vesalio Announces FDA Approval of the NeVa VS™ to Treat Cerebral Vasospasm After Aneurysmal Rupture

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Nashville, TN, September 15, 2022 –(PR.com)– Vesalio announces FDA HDE approval for commercialization of NeVa VS, indicated for the adjunct treatment of symptomatic cerebral vasospasm (CV) following aneurysmal subarachnoid hemorrhage (aSAH), the major cause of death and disability in this patient population. This is the first intracranial technology approved for this indication in the U.S.

CV is a potentially reversible life-threatening condition typically peaking 7 to 10 days after an intracranial hemorrhage caused by aneurysmal rupture (SAH). Vasospasm is the most common complication of SAH with occurrence rates of up to 70% according to publications. It is also known to be the leading cause of delayed morbidity and mortality.

To address this deadly condition, Vesalio leveraged expertise gained through the development of the NeVa™ stent retriever for thrombectomy in acute ischemic stroke. The NeVa VS is a proprietary device…

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