Ignite Creation Date:
2024-05-05 @ 7:19 PM
Last Modification Date:
2024-10-26 @ 9:46 AM
Study NCT ID:
NCT00642876
Status:
COMPLETED
Last Update Posted:
2023-05-10
First Post:
2008-03-19
Brief Title:
PRESTIGE Cervical Disc Study
Sponsor:
Medtronic Spinal and Biologics
Organization:
Medtronic Spinal and Biologics
Study Overview
Official Title:
Investigation of the PRESTIGE Cervical Disc Device at a Single Level for Symptomatic Cervical Disc Disease
Status:
COMPLETED
Status Verified Date:
2023-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this clinical investigation is to evaluate the safety and effectiveness of the ACD in the single level surgical treatment of patients with symptomatic cervical degenerative disc disease The primary follow-up information obtained from this clinical investigation are used to support a PMA application for the ACD
Detailed Description:
None
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