K-number	K103660
Device name	LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
Applicant	Lanx, Inc.
Product code	ODP
Device class	Class II
Decision date	Feb 28, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

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