Southern Spine's C-Fuse Intervertebral Fusion System Receives FDA 510(k) Approval

The FDA granted Macon, Ga.-based Southern Spine 510(k) clearance for its C-Fuse cervical intervertebral body fusion system, according to the Atlanta Business Chronicle. In April, the device maker launched its CE Mark and FDA-approved StabiLink MIS Spinal Fixation System.

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