FDA 510(k) Applications Submitted by Vesatek, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200120 | 01/21/2020 | LiteSaber Wire Torque Assist Device | Vesatek, LLC |
| K170684 | 03/07/2017 | Firebow Wire Torque Assist Device | Vesatek, LLC |
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