K-number	K120509
Device name	STRYKER ALL SUTURE ANCHORS
Applicant	Stryker
Product code	MBI
Device class	Class II
Decision date	Jul 26, 2012
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER ALL SUTURE ANCHORS

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