U.S., Jan. 28 -- ClinicalTrials.gov registry received information related to the study (NCT07370493) titled 'Retrospective Analysis of Patients Implanted With 2 Levels of Prodisc(R) C Vivo Devices' on Nov. 13, 2025.
Brief Summary: The objective of the study is to evaluate the safety and post-operative performance profile of the prodisc(R) C Vivo after implantation in comparison to the relevant clinical literature.
Study Start Date: Nov. 01, 2025
Study Type: OBSERVATIONAL
Condition:
Degenerative Disc Disease
Cervical Spine Degenerative Disease
Symptomatic Cervical Disc Disease
Cervical Spine Degenerative Disc Disease
Intervention:
DEVICE: Prodisc C Vivo
The prodisc(R) C Vivo device is a non-keeled cervical disc replacement prosthesis...