K-number	K241517
Device name	Q Guidance System; Mako Spine System;
Applicant	Stryker Leibinger GmbH & Co KG
Product code	OLO
Device class	Class II
Decision date	Aug 27, 2024
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Q Guidance System; Mako Spine System;

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