K-number	K163621
Device name	Vitoss Bioactive (BA) Injectable
Applicant	Orthovita, Inc.
Product code	MQV
Device class	Class II
Decision date	May 2, 2017
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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Vitoss Bioactive (BA) Injectable

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