FDA clears Sail Fusion’s BowTie Sacroiliac Fusion System
April 23, 2024
Sail Fusion today announced it received FDA 510(k) clearance for its BowTie Sacroiliac Fusion System.
Sail Fusion today announced it received FDA 510(k) clearance for its BowTie Sacroiliac Fusion System.
Front Line Medical Technologies today announced it received CE mark approval for its COBRA-OS device.
Penumbra (NYSE:PEN) announced today that it received FDA clearance for and began the launch of its Lightning Flash 2.0 CAVT system.