K-number	K102265
Device name	LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
Applicant	Ldr Spine USA
Product code	KWQ
Device class	Class II
Decision date	Sep 29, 2010
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM

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