United States — Food and Drug Administration & Medtronic
3 shared events · Importance 3 · Last updated Jun 05, 2026
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United States — Food and Drug Administration: The United States — Food and Drug Administration is the regulatory body to which CereVasc will submit a Premarket Approval (PMA) for its eShunt System, a critical step for commercialization in the US.
Medtronic: Medtronic participated in the Series C financing, showing its interest in CereVasc's eShunt System and potentially expanding its portfolio in neurological medical devices.
Jun 04, 2026 · 6 articles
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