K-number	K101682
Device name	S 100 PEDICLE SCREW SYSTEM
Applicant	Renovis Surgical Technologies, LLC
Product code	MNI
Device class	Class II
Decision date	Dec 7, 2010
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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S 100 PEDICLE SCREW SYSTEM

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