K-number	K153720
Device name	ENZA Zero-Profile Anterior Interbody Fusion
Applicant	Camber Spine Technologies
Product code	OVD
Device class	Class II
Decision date	May 3, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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ENZA Zero-Profile Anterior Interbody Fusion

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