K-number	K072672
Device name	SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
Applicant	Abbott Spine, Inc.
Product code	NKB
Device class	Class II
Decision date	Nov 28, 2007
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES

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