Multi-center, Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial Comparing Mobi-C Cervical Artificial Disc to Anterior Discectomy and Fusion in the Treatment of Symptomatic Degenerative Disc Disease in the Cervical Spine

@inproceedings{Hisey2014MulticenterPR,
  title={Multi-center, Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial Comparing Mobi-C Cervical Artificial Disc to Anterior Discectomy and Fusion in the Treatment of Symptomatic Degenerative Disc Disease in the Cervical Spine},
  author={Michael S. Hisey and Hyun W Bae and Reginald J. Davis and S. Gaede and Greg Hoffman and Kee Duk Kim and Pierce Dalton Nunley and Daniel L Peterson and Ralph F. Rashbaum and John K Stokes},
  booktitle={International journal of spine surgery},
  year={2014}
}
BACKGROUND Anterior cervical discectomy and fusion (ACDF) is the gold standard for treating symptomatic cervical disc degeneration. Cervical total disc replacements (TDRs) have emerged as an alternative for some patients. The purpose of this study was to evaluate the safety and effectiveness of a new TDR device compared with ACDF for treating single-level cervical disc degeneration. METHODS This was a prospective, randomized, controlled, multicenter Food and Drug Administration (FDA… CONTINUE READING

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