Solitaire™ X

3mm vascularization device

XS size

XL confidence

Broadening treatment to smaller vessels.

The new 3mm stent retriever is the latest advancement to the Solitaire™ X portfolio.

Ultra-precision to treat in smaller vessels*

Reach more distal clots with less vessel movement. The 3mm Solitaire™ X Revascularization Device is available in 3x20 and 3x40 enabling ultra-precision for the safe treatment of vessels down to 1.0mm and out to M2^.*,1,2,3

Watch the video and see how the Solitaire™ 3mm performs as compared to the Trevo™* NXT in in-vitro testing.^1,2,3

The 3mm Solitaire™ X device provides a 71% decrease in vessel movement when compared to the competition.¹

Navigate complex anatomy

Solitaire™ X 3mm vs. Trevo™* NXT

Decreased vessel movement in 3 separate in-vitro trials¹
Lower delivery force in an 0.017” microcatheter
Gradually increasing radial force
Longer working length in smaller vessels

Deliver with choice

Greater procedural versatility helping you to operate nimbly²

Deploy with confidence

Designed for safely treat vessels down to 1.0mm with ultra-precision and maintain vessel integrity^1,2,3

Retrieve with control

Minimized vessel movement.
Treat out to M2**^,2,3

Comprehensive Acute
Ischemic Stroke Portfolio

Solitaire™ X is integral in Medtronic’s wide-ranging AIS portfolio, offering responsive and complete solutions to better support your AIS patients.

Solitaire™ X works alongside a collection of agile products to deliver combination therapy as a proven data-backed approach.¹

Our AIS portfolio features state-of-the-art products to enhance your AIS clinical offering:

• Phenom™ 21 and Phenom™ 27 Catheter

• React™ 68 and React™ 71 Catheter

• Riptide™ Aspiration System

• Cello™ Balloon Guide Catheter*

Contact and connect

Reach out if you have questions or need more information

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All charts and percentages are calculated averages observed in bench studies.

* Ultra-Precision as defined by 3mm compared to 4mm, 6mm.
** Compared with Trevo NXT ProVue Retriever

References

D00419703 Rev A
EU IFU (M009589CDOC2, M009589CDOC4)
D00324045 Rev A

See the device manual for detailed information regarding the instructions for use, indications, contraindications, warnings, precautions, and potential adverse events. For further information, contact your local Medtronic representative and/or consult the Medtronic website at medtronic.eu