Precision Spine Nabs FDA OK for Degenerative Disc Disease Implant

Precision Spine’s Dakota anterior cervical discectomy and fusion (ACDF) implant has been granted FDA 510(k) marketing clearance for treating degenerative disc disease.

The system uses a titaniumplate polyetheretherketone (PEEK) cage with cortical cancellous screws to provide maximum support and has a large cavity that promotes natural bone fusion.

With the clearance, the implant system is now indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine in the C2-T1 vertebrae.