K-number	K990959
Device name	K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM
Applicant	Spineology, Inc.
Product code	KWQ
Device class	Class II
Decision date	Dec 27, 1999
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM

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