Stent retrievers
Trevo NXT
A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.
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Where to buy Trevo NXT
Contact Stryker Corporation directly; they can quote, ship, or point you to the distributor for your country.
From stryker.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Trevo NXT 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 |
|---|---|---|---|
| 90312 | Stent Length 32.0 mm | Not stated | Available |
| 90313 | Stent Length 28.0 mm | Not stated | Available |
| 90314 | Stent Length 41.0 mm | Not stated | Available |
| 90315 | Stent Length 37.0 mm | Not stated | Available |
FDA clearances
- 510(k) K223305 March 2023
- 510(k) K210502 August 2021
- 510(k) K203219 December 2020
- 510(k) K200117 February 2020
- 510(k) K192207 November 2019
Procedures that use stent retrievers
Frequently asked questions
What is Trevo NXT used for?
A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.
Who makes Trevo NXT?
Trevo NXT is made by Stryker Corporation. It is listed under stent retrievers for stroke in our device library.
What sizes does Trevo NXT come in?
Sizes listed for Trevo NXT: Stent Length: 28–41 mm. Confirm availability with the manufacturer's instructions for use.
Is Trevo NXT MRI safe?
The FDA device database entry for Trevo NXT does not state its MRI safety status. Check the labeling before MRI.
Is Trevo NXT FDA cleared?
Trevo NXT is covered by FDA submissions K192207, K200117, K203219, K210502, K223305.
How do I contact a Stryker Corporation sales representative?
Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker 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.