Accelus Receives U.S. FDA 510(k) Clearance for its Toro-L Interbody Fusion System
PALM BEACH GARDENS, Fla., May 19, 2022 (GLOBE NEWSWIRE) – Accelus, a privately held medical technology company focused on accelerating the adoption of minimally invasive surgery (MIS) as the standard of care in spine, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Toro Lateral (Toro-L) …
Accelus Receives U.S. FDA 510(k) Clearance for its Toro-L Interbody Fusion System Read More »