Atherectomy
Turbo-Power
A sterile, flexible tube intended to be connected to an atherectomy laser system to invasively direct and deliver laser energy into the peripheral vasculature for the intraluminal photoablation or debulking of lesion material (blockages or total occlusions), to re-establish blood flow within the vessel. It typically consists of fibreoptic materials with a laser-firing distal end and may be designed for over-the-wire (OTW) or rapid exchange insertion. This is a single-use device.
Turbo-Power 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 |
|---|---|---|---|
| 420-050 | Outer Diameter 2.0 mm | Not stated | Available |
| 420-050AA | Outer Diameter 2.0 mm | Not stated | Available |
| 423-050 | Outer Diameter 2.3 mm | Not stated | Available |
| 423-050AA | Outer Diameter 2.3 mm | Not stated | Available |
FDA clearances
- 510(k) K162561 January 2017
- 510(k) K152181 November 2015
Procedures that use atherectomy
Frequently asked questions
What is Turbo-Power used for?
A sterile, flexible tube intended to be connected to an atherectomy laser system to invasively direct and deliver laser energy into the peripheral vasculature for the intraluminal photoablation or debulking of lesion material (blockages or total occlusions), to re-establish blood flow within the vessel. It typically consists of fibreoptic materials with a laser-firing distal end and may be designed for over-the-wire (OTW) or rapid exchange insertion. This is a single-use device.
Who makes Turbo-Power?
Turbo-Power is made by Spectranetics Corporation. It is listed under atherectomy devices in our device library.
What sizes does Turbo-Power come in?
Sizes listed for Turbo-Power: Outer Diameter: 2–2.3 mm. Confirm availability with the manufacturer's instructions for use.
Is Turbo-Power MRI safe?
The FDA device database entry for Turbo-Power does not state its MRI safety status. Check the labeling before MRI.
Is Turbo-Power FDA cleared?
Turbo-Power is covered by FDA submissions K152181, K162561.
How do I contact a Spectranetics Corporation sales representative?
Spectranetics Corporation has not listed representatives on LA Vascular yet. Visit the Spectranetics Corporation 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.