K-number	K120760
Device name	LDR SPINE SPINETUNE TL SPINAL SYSTEM
Applicant	Ldr Spine USA, Inc.
Product code	MNH
Device class	Class II
Decision date	Jun 27, 2012
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LDR SPINE SPINETUNE TL SPINAL SYSTEM

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