K-number	K111848
Device name	EXETER X3 RIMFIT ACETABULAR CUP
Applicant	Stryker Corp.
Product code	JDI
Device class	Class II
Decision date	Oct 5, 2011
Decision	Substantially Equivalent
Regulation	888.3350

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Source

View the full FDA submission: accessdata.fda.gov

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EXETER X3 RIMFIT ACETABULAR CUP

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