K-number	K090669
Device name	RIGIDFIX BIOCRYL CROSS PIN KITS
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	MAI
Device class	Class II
Decision date	Apr 3, 2009
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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RIGIDFIX BIOCRYL CROSS PIN KITS

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