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Voyant 5mm Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K172624
510(k) Type
Special
Applicant
Applied Medical Resources Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2018
Days to Decision
165 days
Submission Type
Summary

Voyant 5mm Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K172624
510(k) Type
Special
Applicant
Applied Medical Resources Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2018
Days to Decision
165 days
Submission Type
Summary