K-number	K113285
Device name	LDR SPINE USA AVENUE L INTERBODY FUSION
Applicant	Ldr Spine USA, Inc.
Product code	OVD
Device class	Class II
Decision date	Jul 26, 2012
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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LDR SPINE USA AVENUE L INTERBODY FUSION

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