K-number	K140879
Device name	BIOSURE HEALICOIL PK INTERFERENCE SCREW
Applicant	Smith & Nephew, Inc.
Product code	MBI
Device class	Class II
Decision date	Jul 21, 2014
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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BIOSURE HEALICOIL PK INTERFERENCE SCREW

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