Viewing Study NCT00758719


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Study NCT ID: NCT00758719
Status: None
Last Update Posted: 2020-02-24 00:00:00
First Post: 2008-09-09 00:00:00
Is Possible Gene Therapy: False
Has Adverse Events: False

Brief Title: Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System
Sponsor: None
Organization:

Study Overview

Official Title: A Prospective Multicenter Lumbar Spine Fusion Study to Evaluate the Effectiveness of the Biomet Lumbar Spinal Fusion System
Status: None
Status Verified Date: 2020-02
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: All subjects enrolled in this study will receive the The Biomet Osteobiologic Treatment System which is comprised of the SpF® Spine Fusion Stimulator and any or all of the following can be utilized in the study: any Pedicle Screw System, autograft and an Interbody Spacer
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?: