K-number	K080728
Device name	LDR SPINE ROI-C IMPLANT
Applicant	Ldr Spine USA
Product code	MQP
Device class	Class II
Decision date	May 29, 2008
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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LDR SPINE ROI-C IMPLANT

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