Stryker Neurovascular | Excelsior™ XT-17™ Microcatheter

Excelsior XT-17 Microcatheter provides smooth tracking, stable delivery and a versatile platform.

Features and benefits

For ease of use. Cross-Helix braid technology and stable durometer produces smooth and balanced tracking through tortuous anatomy.

Cross-Helix XT-braid, resistant durometer, and large ID make XT-17 Microcather a stable delivery platform for therapeutic agents such as coils.

The XT-17 Microcather is compatible with all Stryker non-fibered coils, DMSO*, and therapeutic agents such as PVA particles.

^*Compatibility with individual agents suspended in DMSO has not been established

Specifications

Description	Total/Distal length	Proximal/Distal OD	Proximal/Distal ID
XT-17 Standard Straight, 2-Tip Marker	150cm/7.5cm	2.4F/1.7F 0.80mm/0.60mm	0.017in/0.017in 0.43mm/0.43mm
XT-17 Standard Pre-Shaped 45, 2 Tip Marker	150cm/7.5cm
XT-17 Standard Pre-Shaped 90, 2-Tip Marker	150cm/7.5cm
XT-17 Standard Pre-Shaped J, 2-Tip Marker	150cm/7.5cm
XT-17 Standard Flex Straight, 2-Tip Marker	150cm/15.0cm
XT-17 Standard Flex Pre-Shaped 45, 2-Tip Marker	150cm/15.0cm
XT-17 Flex Pre-Shaped 90, 2-Tip Marker	150cm/15.0cm
XT-17 Flex Pre-Shaped J, 2-Tip Marker	150cm/15.0cm

Compatibility

Effective length	Max catheter shaft OD	Min catheter shaft OD	Proximal/Distal ID	Recommended max guidewire diameter
150cm	2.4F (0.80mm)	1.7F (0.60mm)	0.017in (0.43mm)	Stryker Neurovascular 0.014in (0.36mm)

Looking for more information about this product? Please contact your local sales representative.

See package insert for complete indications, complications, warnings, and instructions for use. (Uploaded on 21/5/2018.)

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THIS CONTENT IS INTENDED SOLELY FOR THE USE OF HEALTHCARE PROFESSIONALS. A physician must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that physicians be trained in the use of any particular product before using it in a procedure. The information presented is intended to demonstrate the breadth of Stryker product offerings. A physician must always refer to the package insert, product label and/or instructions for use before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/ or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area. The Stryker products listed above are CE marked according to the Medical Device Directive 93/42/EEC.