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Voyant 5mm Fusion Device, Voyant Maryland Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K193292
510(k) Type
Special
Applicant
Applied Medical Resources Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
23 days
Submission Type
Summary

Voyant 5mm Fusion Device, Voyant Maryland Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K193292
510(k) Type
Special
Applicant
Applied Medical Resources Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
23 days
Submission Type
Summary