K-number	K091088
Device name	LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
Applicant	Ldr Spine USA
Product code	ODP
Device class	Class II
Decision date	Jul 14, 2009
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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LDR SPINE CERVICAL INTERBODY FUSION SYSTEM

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