K-number	K090060
Device name	NEXLINK OCT SYSTEM, MODEL 7000 SERIES
Applicant	Abbott Spine, Inc.
Product code	KWP
Device class	Class II
Decision date	Jun 2, 2009
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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NEXLINK OCT SYSTEM, MODEL 7000 SERIES

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