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

… The Incidence of Symptomatic Adjacent Segment Disease Requiring Treatment: Cervical
Arthroplasty versus ACDF Jacqueline Myer1, William Beutler, MD, FACS2, Jeffrey R …

Methods Criteria for study participation included symptomatic cervical disc disease in one
vertebral level between C3 and C7, defined by neck and/or arm pain, herniated nucleus …

Probiotics have shown to be beneficial to aquatic farming in aspects such as growth and
development. This study, using three commercial aquaculture species, intends to ascertain if …

Purpose Outcomes are presented for enrolled and treated patients who reached 24 months
post-op in a clinical trial that is being conducted to evaluate the safety and effectiveness of …

Purpose The rate of secondary surgery at the index and adjacent levels was compared
between patients treated with the SECURE®-C Cervical Artificial Disc and ACDF.

BACKGROUND CONTEXT: The safety and efficacy of the SECURE-C Cervical Artificial
Disc were established through a prospective, randomized clinical investigation of the device. …

Purpose The ACADIA Facet Replacement system is being evaluated for safety and
effectiveness in an Investigational Device Exemption (IDE) study. Outcomes are presented …

Purpose Overall success data is presented for enrolled and treated patients who reached 24
month follow-up in a US IDE clinical trial that was conducted to evaluate the safety and …

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 …