K-number	K141217
Device name	ACCULIF TL AND PL CAGE
Applicant	Stryker Corporation
Product code	MAX
Device class	Class II
Decision date	Jul 16, 2014
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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ACCULIF TL AND PL CAGE

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