K-number	K220593
Device name	Spine Guidance Software, Stryker Q Guidance System
Applicant	Stryker Leibinger GmbH & Co KG
Product code	OLO
Device class	Class II
Decision date	May 27, 2022
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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Spine Guidance Software, Stryker Q Guidance System

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