K-number	K092631
Device name	MANTIS REDUX SPINAL SYSTEM
Applicant	Stryker Spine
Product code	NKB
Device class	Class II
Decision date	Sep 25, 2009
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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MANTIS REDUX SPINAL SYSTEM

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