K-number	K062666
Device name	VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS
Applicant	Ortho Development Corp.
Product code	MQP
Device class	Class II
Decision date	Jan 25, 2007
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS

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