K-number	K071905
Device name	POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
Applicant	Lanx, LLC
Product code	KWQ
Device class	Class II
Decision date	Dec 28, 2007
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)

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