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Study identifier: NCT04982835 Synced from ClinicalTrials.gov · August 05, 2026
● Active Not Recruiting

M6-C Artificial Cervical Disc Two-Level IDE Pivotal Study

Condition: Cervical Disc Degenerative Disorder  ·  Sponsor: Orthofix Inc.

PhaseNA
Planned participants156
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Prospective, concurrently controlled, multi-center study to evaluate the safety and effectiveness of the Spinal Kinetics M6-C™ artificial cervical disc compared to anterior cervical discectomy and fusion (ACDF) for the treatment of contiguous two-level symptomatic cervical radiculopathy at vertebral levels from C3 to C7 with or without spinal cord compression.

This description comes directly from the study's public registry record.

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No contact information is available for this study as per the public registry record.

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Locations (21)

Desert Institute for Spine CarePhoenix, Arizona, United States
Beverly Hills Spine SurgeryBeverly Hills, California, United States
Memorial Orthopaedic Surgical GroupLong Beach, California, United States
Disc Sports & Spine CenterNewport Beach, California, United States
UC Irvine Medical CenterOrange, California, United States
Institute of Neuro InnovationSanta Monica, California, United States
St. Charles Spine InstituteThousand Oaks, California, United States
University of Colorado School of Medicine - Department of OrthopedicsAurora, Colorado, United States
Steadman Philipon Research InstituteVail, Colorado, United States
Orlando HealthOrlando, Florida, United States
Joseph Spine InstituteTampa, Florida, United States
Longstreet ClinicGainesville, Georgia, United States

+ 9 more locations — full list on the registry record.

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