K-number	K223553
Device name	Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine
Applicant	Brainlab AG
Product code	OLO
Device class	Class II
Decision date	Aug 2, 2023
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine

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