Ignite Creation Date:
2024-05-05 @ 4:40 PM
Last Modification Date:
2024-10-26 @ 9:23 AM
Study NCT ID:
NCT00292292
Status:
TERMINATED
Last Update Posted:
2013-09-13
First Post:
2006-02-13
Brief Title:
Kineflex Artificial Disc System to Treat Degenerative Disc Disease DDD
Sponsor:
SpinalMotion
Organization:
SpinalMotion
Study Overview
Official Title:
Clinical Study Protocol for the Investigation of the Kineflex Spinal System - a Pivotal Study in Continued Access Stage
Status:
TERMINATED
Status Verified Date:
2013-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Economic and business reasons
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The Kineflex Spinal System is no worse than the Charite Spinal System in patients with single level degenerative disc disease at L45 or L5S1
Detailed Description:
The Kineflex disc is a 3-piece modular design consisting of 2 cobalt chrome molybdenum CCM end-plates and a fully articulating CCM core The system is available in 3 foot print sizes
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None