K-number	K140531
Device name	BIOFOAM BONE WEDGE
Applicant	Wrightmedicaltechnologyinc
Product code	HRS
Device class	Class II
Decision date	Jul 9, 2014
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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BIOFOAM BONE WEDGE

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