K-number	K122989
Device name	BIOMET LATERAL SPACER SYSTEM
Applicant	Biomet Spine (Aka Ebi, LLC)
Product code	MAX
Device class	Class II
Decision date	Oct 24, 2012
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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BIOMET LATERAL SPACER SYSTEM

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