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Voyant Fine Fusion Device (EB230)

Page Type
Cleared 510(K)
510(k) Number
K202818
510(k) Type
Traditional
Applicant
Applied Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
448 days
Submission Type
Summary

Voyant Fine Fusion Device (EB230)

Page Type
Cleared 510(K)
510(k) Number
K202818
510(k) Type
Traditional
Applicant
Applied Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
448 days
Submission Type
Summary