K-number	K120802
Device name	ORTHOLOC(TM) 3DI LOCKING SCREWS ORTHOLOC(TM) BONE SCREWS
Applicant	Wrightmedicaltechnologyinc
Product code	HRS
Device class	Class II
Decision date	Apr 2, 2012
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOLOC(TM) 3DI LOCKING SCREWS ORTHOLOC(TM) BONE SCREWS

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