K-number	K991089
Device name	SYNTHES CERVIFIX SYSTEM
Applicant	Synthes Spine
Product code	KWP
Device class	Class II
Decision date	Aug 27, 1999
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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SYNTHES CERVIFIX SYSTEM

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