K-number	K062173
Device name	MODIFICATION TO BONE GRAFT SYRINGE
Applicant	Wrightmedicaltechnologyinc
Product code	FMF
Device class	Class II
Decision date	Aug 23, 2006
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO BONE GRAFT SYRINGE

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