SpineGuard Receives 510(k) Clearance to Market PediGuard Threaded DSG
SpineGuard received FDA 510(k) clearance to market the PediGuard Threaded DSG™ device for Dynamic Surgical Guidance. The system supports open or minimally invasive approaches for pedicle screw insertion.
The system launched in the EU and Asia earlier this year, following approval under the CE Mark.
Sources: SpineGuard, ORTHOWORLD Inc.