K-number	K203327
Device name	VERTACONNECT TLIF Cage
Applicant	Signus Medizintechnik
Product code	MAX
Device class	Class II
Decision date	Jan 25, 2021
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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VERTACONNECT TLIF Cage

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