K-number	K202818
Device name	Voyant Fine Fusion Device (EB230)
Applicant	Applied Medical
Product code	GEI
Device class	Class II
Decision date	Dec 16, 2021
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Voyant Fine Fusion Device (EB230)

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