K-number	K121096
Device name	VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
Applicant	L&K BIOMED Co., Ltd.
Product code	MAX
Device class	Class II
Decision date	Jul 6, 2012
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM

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