K-number	K220696
Device name	uCerv Flux-C 3D Porous Titanium Cervical Interbody
Applicant	Ulrich Medical USA
Product code	ODP
Device class	Class II
Decision date	Aug 19, 2022
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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uCerv Flux-C 3D Porous Titanium Cervical Interbody

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