K-number	K240582
Device name	VEA Align; spineEOS
Applicant	Eos Imaging
Product code	QIH
Device class	Class II
Decision date	Jun 25, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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VEA Align; spineEOS

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