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Voyant Maryland Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K182653
510(k) Type
Special
Applicant
Applied Medical Resources Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2018
Days to Decision
50 days
Submission Type
Summary

Voyant Maryland Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K182653
510(k) Type
Special
Applicant
Applied Medical Resources Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2018
Days to Decision
50 days
Submission Type
Summary