K-number	K102957
Device name	CUTTING EDGE SPINE INTERBODY FUSION DEVICE
Applicant	Cutting Edge Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Apr 28, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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CUTTING EDGE SPINE INTERBODY FUSION DEVICE

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