Borvo EVAC™ System Provides Advanced Approach for the Growing Number of PatientsRequiring Subdural Hematoma (SDH) Drainage Driven by Factors Such as Head Injuries and an Aging Population
MOUNTAIN VIEW, Calif., Oct. 08, 2024 (GLOBE NEWSWIRE) -- Borvo Medical, a neurointerventional medtech startup, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance of the Borvo (Endoport Vacuum Assisted Collection) EVAC™ system, an advanced alternative to traditional subdural hematoma (SDH) drainage methods. The Company will present its innovative technology later today at the 17th World Federation of Interventional and Therapeutic Neuroradiology (WFITN) Congress, taking place in New York from October 6-10, 2024. Designed to address the limitations of existing devices, Borvo EVAC leverages state-of-the-art fabrication techniques, improved materials science, and ergonomic designs to provide a modernized, efficient, and less invasive solution. The EVAC meets the evolving needs of an aging population and individuals requiring SDH drainage due to head injuries and other causes. The EVAC system is anticipated to be available in early 2025.
"Borvo EVAC represents a significant advancement in the approach to treating subdural hematoma. For years, clinicians have relied on traditional devices such as the stainless-steel Subdural Evacuation Port System (SEPS), which, while effective, have not evolved to meet modern demands, including imaging compatibility. Our technology not only addresses ...
