K-number	K193129
Device name	Yukon OCT Spinal System
Applicant	K2m, Inc.
Product code	NKG
Device class	Class II
Decision date	Feb 7, 2020
Decision	Substantially Equivalent
Regulation	888.3075

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Source

View the full FDA submission: accessdata.fda.gov

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Yukon OCT Spinal System

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