K-number	K113642
Device name	PERIMETER INTERBODY FUSION DEVICE
Applicant	Medtronic Sofamor Danek USA
Product code	MAX
Device class	Class II
Decision date	Feb 6, 2012
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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PERIMETER INTERBODY FUSION DEVICE

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