K-number	K222015
Device name	Integral Titanium Cervical Interbody
Applicant	Nvision Biomedical Technologies, Inc.
Product code	ODP
Device class	Class II
Decision date	Jul 5, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Integral Titanium Cervical Interbody

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