Study Design. Prospective, multicenter, randomized, and controlled Investigational Device
Exemption clinical trial. Objective. To compare the clinical safety and effectiveness of the …

Background: This research was initiated to compare the long-term clinical safety and effectiveness
of the selectively constrained SECURE-C (Globus Medical, Audubon, Pennsylvania) …

✓ Compression of the spinal cord or nerve roots resulting from degenerative spondylosis is
commonly seen in the cervical or lumbar region, but it has not previously been described in …

Purpose The design of this IDE study is to investigate the clinical results of traditional ACDF
versus a cervical arthroplasty device.

BACKGROUND CONTEXT: Long-term follow-up is essential to understand the effects of
semi-constrained cervical arthroplasty on patients. Data from 2-3 year post-op visits is …

BACKGROUND CONTEXT: Cervical disc arthroplasty has become an alternative to fusion
in patients with symptomatic cervical disc disease. PURPOSE: This study compares clinical …

BACKGROUND CONTEXT: Cervical disc arthroplasty is intended to maintain motion of the
cervical spine following discectomy rather than traditional fusion which immobilizes the …

BACKGROUND CONTEXT: While anterior cervical discetomy and fusion (ACDF) provides
rigid fixation increasing the likelihood of bony fusion and pain reduction in patients with …

Purpose The clinical results of a semi-constrained cervical arthroplasty device using the
SECURE®-C Cervical Artificial Disc (Globus Medical, Audubon, PA) were compared with that of …

Purpose Five year follow-up data are presented for patients treated in the SECURE®-C IDE
study.