K-number	K172212
Device name	MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK
Applicant	Ctl Medical Corporation
Product code	ODP
Device class	Class II
Decision date	Jan 9, 2018
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK

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MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK