K-number	K121670
Device name	MEDYSSEY CANNULATED PEDICLE SCREW
Applicant	Medyssey Co, Ltd.
Product code	NKB
Device class	Class II
Decision date	Jan 25, 2013
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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MEDYSSEY CANNULATED PEDICLE SCREW

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