K-number	K110650
Device name	ZYSTON ARC INTERBODY SPACER
Applicant	Biomet Spine (Aka Ebi, LLC)
Product code	MAX
Device class	Class II
Decision date	Jun 30, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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ZYSTON ARC INTERBODY SPACER

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