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Clinical Trial Summary

This clinical study will assess the metal concentrations present in the blood serum of patients who receive surgical treatment with the PRESTIGE LP™ Cervical Disc at two contiguous cervical levels from C3-C7. The information obtained from this clinical investigation will be used to support the post market surveillance for a PMA supplement for the PRESTIGE LP™ Cervical Disc implanted at two contiguous levels.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03062657
Study type Interventional
Source Medtronic Spinal and Biologics
Contact
Status Terminated
Phase N/A
Start date June 6, 2018
Completion date January 27, 2023

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