K-number	K110046
Device name	ATHENA PEDICLE SCREW SYSTEM
Applicant	Royal Oak Medical Devices
Product code	NKB
Device class	Class II
Decision date	Dec 7, 2011
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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ATHENA PEDICLE SCREW SYSTEM

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