Headquarters
San Jose, CA
Industry
Life Sciences – Medical Device – Spinal
Overview
DFine’s RF Kyphoplasty procedure with the StabiliT™ Vertebral Augmentation System is the next generation in kyphoplasty. The first RF Kyphoplasty cases were conducted in Europe as part of the SPACE clinical study in December of 2006. US spine specialists began performing RF Kyphoplasty with the StabiliT™ Vertebral Augmentation System in April of 2008, while commercialization in Europe began in February of 2009.
Solution
QAD Enterprise Applications was implemented to help Dfine prepare systems for product commercialization and to establish a robust enterprise infrastructure for expansion and growth.
Results
While using QAD and Strategic DFine has commercialized their product in Europe.
