K-number	K103040
Device name	LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
Applicant	Lanx, LLC
Product code	NKB
Device class	Class II
Decision date	Feb 8, 2011
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)

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