K-number	K113871
Device name	PRO-DENSE BONE GRAFT SUBSTITUTE
Applicant	Wrightmedicaltechnologyinc
Product code	MQV
Device class	Class II
Decision date	Mar 25, 2013
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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PRO-DENSE BONE GRAFT SUBSTITUTE

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