K-number	K190556
Device name	Zimmer Biomet Universal Navigation System
Applicant	Zimmer Biomet Spine, Inc.
Product code	OLO
Device class	Class II
Decision date	Oct 24, 2019
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Zimmer Biomet Universal Navigation System

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