K-number	K180459
Device name	VERASENSE for Zimmer Biomet Persona
Applicant	Orthosensor, Inc.
Product code	ONN
Device class	Class II
Decision date	Jun 7, 2018
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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VERASENSE for Zimmer Biomet Persona

Everything you need for a 510(k) submission. Nothing you don't.