K-number	K071520
Device name	RENOVO SUTURE ANCHORS, MODELS 100-2001 THRU 100-5502X
Applicant	Core Essence Orthopaedics, LLC
Product code	MBI
Device class	Class II
Decision date	Aug 10, 2007
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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RENOVO SUTURE ANCHORS, MODELS 100-2001 THRU 100-5502X

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