NCT01832818View on ClinicalTrials.gov

Post-Market Study Evaluating the Safety and Effectiveness of NuNec® Cervical Arthroplasty System

NATerminatedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

January 31, 2016

Study Completion Date

January 31, 2016

Conditions
Cervical Intervertebral Disc Degeneration
Interventions
DEVICE

NuNec Cervical Disc

Patients will be enrolled and implanted with the NuNec device at a single level C3 to C7.

Trial Locations (1)

Unknown

University Hospital of North Tees, Stockton-on-Tees

Sponsors
All Listed Sponsors
lead

Pioneer Surgical Technology, Inc.

INDUSTRY

NCT01832818 - Post-Market Study Evaluating the Safety and Effectiveness of NuNec® Cervical Arthroplasty System | Biotech Hunter | Biotech Hunter