LDR's ROI-C Cervical Cage has received FDA clearance for use with allograft.
Here are four points:
1. Previously, the ROI-C Cervical Cage was cleared only for use with autogenous bone graft.
2. LDR presented clinical literature review data to the FDA to investigate the risks and benefits associated with using allogenic bone graft with ROI-C.
3. The system is indicated for use in adult patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level from C2-T1.
4. LDR is a global medical device company focused on designing and commercializing proprietary surgical technologies for spinal treatments.