K-number	K100952
Device name	MODIFICATION TO SYNTHES MATRIX SYSTEM
Applicant	Synthes Spine
Product code	NKB
Device class	Class II
Decision date	Aug 5, 2010
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO SYNTHES MATRIX SYSTEM

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