Atherectomy
Drive System (Straub Medical)
A multi-purpose assembly of devices designed to power and control the mechanical mechanism of an atherectomy and/or thrombectomy catheter (not included) during an intravascular recanalization procedure. It typically consists of an electrically-powered control unit that supplies the drive motor with electricity to power the catheter and a handpiece with hand-switch that includes the drive motor (for catheter manipulation); a foot-switch may also be included. This is a reusable device.
Drive System (Straub Medical) models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| Version 1.0 | — | MR Unsafe | Available |
FDA clearances
- 510(k) K172315 April 2018
Procedures that use atherectomy
Frequently asked questions
What is Drive System (Straub Medical) used for?
A multi-purpose assembly of devices designed to power and control the mechanical mechanism of an atherectomy and/or thrombectomy catheter (not included) during an intravascular recanalization procedure. It typically consists of an electrically-powered control unit that supplies the drive motor with electricity to power the catheter and a handpiece with hand-switch that includes the drive motor (for catheter manipulation); a foot-switch may also be included. This is a reusable device.
Who makes Drive System (Straub Medical)?
Drive System (Straub Medical) is made by Straub Medical AG. It is listed under atherectomy devices in our device library.
What sizes does Drive System (Straub Medical) come in?
The FDA device database does not list sizes for Drive System (Straub Medical). Check the instructions for use or ask a Straub Medical AG representative.
Is Drive System (Straub Medical) MRI safe?
The FDA device database lists Drive System (Straub Medical) as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is Drive System (Straub Medical) FDA cleared?
Drive System (Straub Medical) is covered by FDA submission K172315.
How do I contact a Straub Medical AG sales representative?
Straub Medical AG has not listed representatives on LA Vascular yet. Visit the Straub Medical AG company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.