DynaBridge Staple System – FDA Cleared

After years of development, Fusion Orthopedics is pleased to announce the DynaBridge System as the newest addition to their product offering. FDA 510(k) clearance was issued October 15th, 2018. The assigned FDA 510(k) # for DynaBridge is K181815. The system is indicated for fracture and osteotomy fixation and joint arthrodesis...

TalarLift STS – FDA Cleared

We are pleased to announce the TalarLift STS as the newest addition to the Fusion Orthopedics product offering. FDA 510(k) clearance was issued August 11th, 2017. The assigned FDA 510(k) # for TalarLift STS is K170624. The TalarLift STS is a comprehensive arthroereisis system indicated for use in the treatment...