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Firebow Wire Torque Assist Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170684
510(k) Type
Traditional
Applicant
Vesatek, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2017
Days to Decision
114 days
Submission Type
Summary

Firebow Wire Torque Assist Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170684
510(k) Type
Traditional
Applicant
Vesatek, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2017
Days to Decision
114 days
Submission Type
Summary