Benvenue Medical has enrolled more than 250 patients in the Kiva System as a Vertebral Augmentation Treatment safety and effectiveness trial.
The study will be the largest randomized study to compare the current standard of care to balloon kyphoplasty for treating vertebral compression fractures related to osteoporosis. The IDE study will support a future FDA 510(k) market clearance application.
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More Articles on Orthopedic Devices:
Benvenue Medical Launches Blazer Vertebral Augmentation System
Bacterin Revenue Jumps 96% in 2011
Symmetry Medical Launches 12 Line Enhancements for Retractor System