This study is designed to to assess the safety and efficacy of the DASCOR® Disc Arthroplasty Device in subjects with degenerative disc disease (DDD) of the lumbar spine.
A non-randomized, prospective,
multicenter, evaluation of 20 subjects implanted at up to 10 investigational sites. All subjects chosen to participate in the study will get the DASCOR device.Original post by Ben Parr