K-number	K102331
Device name	LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
Applicant	Ldr Spine USA
Product code	MNI
Device class	Class II
Decision date	Oct 15, 2010
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LDR SPINE USA SPINETUNE TL SPINAL SYSTEM

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