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Voyant Open Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153288
510(k) Type
Traditional
Applicant
Applied Medical Resources
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2016
Days to Decision
201 days
Submission Type
Summary

Voyant Open Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153288
510(k) Type
Traditional
Applicant
Applied Medical Resources
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2016
Days to Decision
201 days
Submission Type
Summary