K-number	K133671
Device name	ICONIX ALL SUTURE ANCHORS
Applicant	Stryker Corp.
Product code	MBI
Device class	Class II
Decision date	Feb 28, 2014
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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ICONIX ALL SUTURE ANCHORS

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