K-number	K111716
Device name	KNOTLESS SUTURE FIXATION SYSTEM
Applicant	Core Essence Orthopaedics
Product code	MBI
Device class	Class II
Decision date	Nov 10, 2011
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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KNOTLESS SUTURE FIXATION SYSTEM

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