Stent retrievers
SolitaireTM
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 SolitaireTM
Contact Micro Therapeutics, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From lavascular.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.
SolitaireTM 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 |
|---|---|---|---|
| SFR3-4-20-05 | — | Not stated | Available |
| SFR3-4-20-10 | — | Not stated | Available |
| SFR3-4-40-10 | — | Not stated | Available |
| SFR3-6-20-10 | — | Not stated | Available |
| SFR3-6-24-06 | — | Not stated | Available |
| SFR3-6-40-10 | — | MR Conditional | Available |
FDA clearances
- 510(k) K160641 March 2017
- 510(k) K161879 September 2016
- 510(k) K153071 December 2015
Procedures that use stent retrievers
Frequently asked questions
What is SolitaireTM 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 SolitaireTM?
SolitaireTM is made by Micro Therapeutics, Inc.. It is listed under stent retrievers for stroke in our device library.
What sizes does SolitaireTM come in?
The FDA device database does not list sizes for SolitaireTM. Check the instructions for use or ask a Micro Therapeutics, Inc. representative.
Is SolitaireTM MRI safe?
The FDA device database lists SolitaireTM as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is SolitaireTM FDA cleared?
SolitaireTM is covered by FDA submissions K160641, K153071, K161879.
How do I contact a Micro Therapeutics, Inc. sales representative?
Micro Therapeutics, Inc. has not listed representatives on LA Vascular yet. Visit the Micro Therapeutics, Inc. 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.