A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.
NCT: NCT04416321 · COMPLETED
NCT IDNCT04416321
StatusCOMPLETED
Start Date2021-07-01
Completion2026-01-27
SponsorInvibio Ltd (INDUSTRY)
First posted
Last updated
Brief Summary
The purpose of this trial is to collect clinical outcomes including radiographic and CT outcomes in patients who undergo spinal fusion using the Keos Lumbar Interbody Fusion Device.
Frequently Asked Questions
What is A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.?
A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced. is a clinical trial registered under NCT04416321. Current status: COMPLETED.
What is the status of NCT04416321?
The current status of NCT04416321 (A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.) is: COMPLETED.
When did A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced. start?
A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced. started on 2021-07-01.
Related Devices
K153107Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine VEO™ Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion SystemChoicespine, LP
K153373CORNERSTONE PSR Cervical Fusion System, PERIMETER C Spinal System, PEEK PREVAIL Cervical Interbody DeviceMedtronic Sofamor Danek
K161404Genesys Spine Apache® Lateral Lumbar Interbody Fusion SystemGenesys Spine
K161438Genesys Spine Apache® Anterior Lumbar Interbody Fusion SystemGenesys Spine
K162103Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Interbody Fusion System (Harrier™), Choice Spine Vertebral Body Replacement System (Hawkeye™)Choicespine, LP
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.