K-number	K103822
Device name	SYNTHES HEMOSTATIC BONE PUTTY (HBP)
Applicant	Synthes USA Products, LLC
Product code	MTJ
Device class	Class U
Decision date	May 19, 2011
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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SYNTHES HEMOSTATIC BONE PUTTY (HBP)

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