K-number	K181606
Device name	Precision Spine Navigation Instrumentation
Applicant	Precision Spine, Inc.
Product code	OLO
Device class	Class II
Decision date	Sep 27, 2019
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Precision Spine Navigation Instrumentation

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