SAIL Fusion Announces FDA Clearance of its BowTie™ Sacroiliac Fusion System
SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon proven AO principles, today announced that it has received FDA clearance for its novel BowTie Sacroiliac Fusion System.
- SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon proven AO principles, today announced that it has received FDA clearance for its novel BowTie Sacroiliac Fusion System.
- The system will be launched to a select group of initial surgeons in preparation for a greater expansion in the coming months.
- “There hasn’t been meaningful differentiation in the SI fusion market for many years,” remarked David Jansen, the President & CEO of SAIL.
- Our approach challenges the prevailing trend of lateral fixation that is more appropriate for stabilization rather than true joint fusion.