Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of the Biomet Lumbar Spinal Fusion System in patients undergoing lumbar fusion surgery.

Clinical Trial Description

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 ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00758719
Study type	Observational
Source	Zimmer Biomet
Contact
Status	Completed
Phase
Start date	September 2008
Completion date	August 2012

View Details

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