
Chaperon™
Guiding Catheters
LVIS™ and LVIS™ Jr. devices are braided coil assist stents used for aneurysm embolization.
The LVIS Device. *The blue wire denotes the radiopaque stent body material
The LVIS Device. *The blue wire denotes the radiopaque stent body material
The LVIS Jr. Device. *The blue wire denotes the radiopaque stent body material
The LVIS Jr. Device. *The blue wire denotes the radiopaque stent body material
The LVIS® Device is compatible with the Headway® 21 Microcatheter
The LVIS® Jr. Device is compatible with the Headway® 17 Microcatheter, Scepter C®, and Scepter XC® Occlusion Balloons.
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Sizes are not approved or available in certain regions. Please contact your local sales representative for region specific sizing
ITT (intended to treat) population N=153. All missing patients were considered failures
All LVIS PMA pivotal study data based on FDA Approval P170013
RR Class 1 (N=111) + RR Class 2 with stable or positive occlusion and no retreatment (N=16). Subjects having negative progression from post-procedure to 12 months or retreatment are considered failures. Missing data imputed as failures
mRS score ≥ 3 at any time point between 90 days and last available follow-up. 2 major strokes were caused by pre-existing morbidities and were in vascular territories unrelated to device or procedure