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Clinical Trial Summary

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for instrumented posterolateral spine fusion, as compared to local autograft.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02018445
Study type Interventional
Source SeaSpine, Inc.
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date May 2017

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