Ignite Creation Date:
2024-05-06 @ 1:47 PM
Last Modification Date:
2024-10-26 @ 1:20 PM
Study NCT ID:
NCT04128852
Status:
WITHDRAWN
Last Update Posted:
2024-02-13
First Post:
2019-10-04
Brief Title:
Post Marketing Clinical Follow up Study for MagnetOs Putty in Patients With Degenerative Disc Disease
Sponsor:
Kuros Biosurgery AG
Organization:
Kuros Biosurgery AG
Study Overview
Official Title:
A Prospective Single Arm Single-center Study to Assess the Safety and Performance of MagnetOs Putty in Patients Undergoing SingleTwo-level Lateral Lumbar Interbody Fusion
Status:
WITHDRAWN
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
redirected funding
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PROGRESS
Brief Summary:
This study is a post-marketing clinical follow-up study for MagnetOs Putty MagnetOs Putty is a synthetic bone-like material which is routinely used by surgeons as a treatment for patients with degenerative disc disease who will undergo surgery for spinal fusion extreme lateral interbody fusion XLIF MagnetOs Putty will be used according to the instructions for use
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None