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Dynesys Spinal System Post Market 522 Study

Degenerative Spondylolisthesis Clinical Trial

Official title:
Post Market Surveillance for the Dynesys Spinal System, Assessing Safety and Fusion.

Clinical Trial Summary

The purpose of this study is to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System used as an adjunct to fusion and compare to literature control.

Clinical Trial Description

Study is meant to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01528072
Study type Interventional
Source Zimmer Biomet
Contact
Status Terminated
Phase N/A
Start date March 2012
Completion date April 2017
View Details
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