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Post Marketing Clinical Follow up Study for MagnetOs Putty in Patients With Degenerative Disc Disease — PROGRESS  

Degenerative Disc Disease Clinical Trial

Official title:
A Prospective, Single Arm, Single-center Study to Assess the Safety and Performance of MagnetOs Putty in Patients Undergoing Single/Two-level Lateral Lumbar Interbody Fusion

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04128852
Study type Interventional
Source Kuros Biosurgery AG
Contact
Status Withdrawn
Phase N/A
Start date November 11, 2020
Completion date December 2023
View Details
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