K-number	K120824
Device name	3.9MM REELX STT SUTURE ANCHOR SYSTEM
Applicant	Stryker Corp.
Product code	MBI
Device class	Class II
Decision date	Jul 18, 2012
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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3.9MM REELX STT SUTURE ANCHOR SYSTEM

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