A Post-Market Study of PEEK-OPTIMA HA Enhanced Keos Lumbar Interbody Fusion Device
Completed Not Applicable NCT04416321
Study Description
A Clinical Study to Evaluate Safety and Performance of a Spinal Fusion Device
Study Details
- Registry ID:
- NCT04416321
- Conditions:
- Degenerative Disc Disease, Spondylolisthesis, Retrolisthesis
- Phase:
- Not Applicable
- Target Enrollment:
- 25 participants
- Start Date:
- Age Range:
- 18–999 years
- Healthy Volunteers:
- No
Study Locations (1 site)
-
Neurosurgical Associates of Lancaster
Lancaster, Pennsylvania, United States
Interested in Participating?
Check your eligibility and learn more about this study on TrialScreen.