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Clinical Trial Summary

This is a multi-center, prospective, outcomes study. In this study, the Zero-P PEEK implant will be used in patients undergoing ACDF for treatment of SCDD at a single level between C3 and C7. The cohort will be followed over time to twenty-four (24) months after surgery. Up to fifteen (15) sites will participate in this study. This is not a controlled study.


Clinical Trial Description

This was a post-market study ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00945243
Study type Interventional
Source Synthes USA HQ, Inc.
Contact
Status Terminated
Phase N/A
Start date July 1, 2009
Completion date December 1, 2011

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