K-number	K234009
Device name	Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)
Applicant	Mighty Oak Medical
Product code	QIH
Device class	Class II
Decision date	Jul 12, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)

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