OBJECTIVE Food and Drug Administration–approved investigational device exemption
(IDE) studies have provided level I evidence supporting cervical disc arthroplasty (CDA) as a …

OBJECT This study compared the safety and efficacy of treatment with the PRESTIGE LP
cervical disc versus a historical control anterior cervical discectomy and fusion (ACDF) …

OBJECTIVE The authors compared the efficacy and safety of arthroplasty using the Prestige
LP cervical disc with those of anterior cervical discectomy and fusion (ACDF) for the …

Background Cervical disc arthroplasty (CDA) has emerged as an alternative to anterior
cervical discectomy and fusion (ACDF) for the treatment of cervical pathologies. Studies are …

OBJECTIVE The authors assessed the 10-year clinical safety and effectiveness of cervical
disc arthroplasty (CDA) to treat degenerative cervical spine disease at 2 adjacent levels …

Object Cervical total disc replacement (TDR) was developed to address some of the
shortcomings associated with anterior cervical discectomy and fusion (ACDF) by preserving …

Object The purpose of this study was to determine long-term clinical outcomes in patients
undergoing anterior cervical surgery in which a cervical disc prosthesis was used to treat …

Background Cervical total disc replacement (TDR) is an increasingly accepted procedure for
the treatment of symptomatic cervical degenerative disc disease. Multiple Level I evidence …

Study Design. Prospective, randomized, single-center, clinical trial. Objective. To
prospectively examine the 7-and 10-year outcomes of cervical arthroplasty to anterior …

Object The authors assess the long-term safety and efficacy of cervical disc replacement
with the Prestige Cervical Disc in a prospective, randomized, multicenter trial at 7 years of …