LVIS & LVIS Jr Clinical Study

Title: “MicroVention Low-Profile Visualized Intraluminal Support (LVIS®) or LVIS Jr® Humanitarian Use Device (LVIS HUD)”

Study Sponsor: MicroVention, Inc.

Principal Investigator: Matthew Lawson, MD

Study Synopsis: The Low-Profile Visualized Intraluminal Support Devises (LVIS & LVIS Jr.) are authorized by the Federal Law for use with bare platinum embolic coils for the treatment of un-ruptured, wide-neck, intracranial, saccular aneurysms from a parent vessel with a diameter of ≥2.5mm and ≤4.5 mm.

The LVIS & LVIS Jr Intraluminal Support Devices have been approved by the Food and Drug Administration (FDA) with a Humanitarian Use Device (HUD) designation. This designation is recognition that the device has a limited patient population of fewer than 4,000 individuals in the United States per year.

Study Status: Only for patients with an un-ruptured, wide neck, intracranial, saccular aneurysm.

For more information, contact Lutheria Hollis, CCRC at (850) 201-2350

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