K-number	K073633
Device name	STRYKER ESSX MICRODEBRIDER SYSTEM
Applicant	Stryker Ireland Ltd., Instruments Division
Product code	ERL
Device class	Class II
Decision date	Aug 26, 2008
Decision	Substantially Equivalent
Regulation	874.4250

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View the full FDA submission: accessdata.fda.gov

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STRYKER ESSX MICRODEBRIDER SYSTEM

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