Flow diverters
Surpass Streamline
A non-bioabsorbable tubular device typically intended to be implanted into the base or parent artery of an intracranial aneurysm (e.g., wide-neck aneurysm situated at the base of a bifurcation) to facilitate the delivery of embolics to fill the aneurysm, facilitate clotting within the aneurysm by slowing blood flow into it, and/or to provide support for a neurovascular embolization coil placed inside the aneurysm. It is made of uncoated metal [e.g., nickel-titanium alloy (Nitinol)] and self-expands after it is delivered to the site of implantation and released (e.g., from a dedicated delivery instrument). Disposable devices associated with implantation may be included.
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Where to buy Surpass Streamline
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.
Surpass Streamline 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 |
|---|---|---|---|
| M003SFD030150 | Length 15.0 mm; Lumen/Inner Diameter 3.0 mm | MR Conditional | Available |
| M003SFD030200 | Length 20.0 mm; Lumen/Inner Diameter 3.0 mm | MR Conditional | Available |
| M003SFD030250 | Length 25.0 mm; Lumen/Inner Diameter 3.0 mm | MR Conditional | Available |
| M003SFD040150 | Lumen/Inner Diameter 4.0 mm; Length 15.0 mm | MR Conditional | Available |
| M003SFD040200 | Lumen/Inner Diameter 4.0 mm; Length 20.0 mm | MR Conditional | Available |
| M003SFD040250 | Length 25.0 mm; Lumen/Inner Diameter 4.0 mm | MR Conditional | Available |
| M003SFD040300 | Length 30.0 mm; Lumen/Inner Diameter 4.0 mm | MR Conditional | Available |
| M003SFD040400 | Length 40.0 mm; Lumen/Inner Diameter 4.0 mm | MR Conditional | Available |
| M003SFD040500 | Length 50.0 mm; Lumen/Inner Diameter 4.0 mm | MR Conditional | Available |
| M003SFD050200 | Length 20.0 mm; Lumen/Inner Diameter 5.0 mm | MR Conditional | Available |
| M003SFD050250 | Lumen/Inner Diameter 5.0 mm; Length 25.0 mm | MR Conditional | Available |
| M003SFD050300 | Length 30.0 mm; Lumen/Inner Diameter 5.0 mm | MR Conditional | Available |
| M003SFD050400 | Length 40.0 mm; Lumen/Inner Diameter 5.0 mm | MR Conditional | Available |
| M003SFD050500 | Length 50.0 mm; Lumen/Inner Diameter 5.0 mm | MR Conditional | Available |
Procedures that use flow diverters
Frequently asked questions
What is Surpass Streamline used for?
A non-bioabsorbable tubular device typically intended to be implanted into the base or parent artery of an intracranial aneurysm (e.g., wide-neck aneurysm situated at the base of a bifurcation) to facilitate the delivery of embolics to fill the aneurysm, facilitate clotting within the aneurysm by slowing blood flow into it, and/or to provide support for a neurovascular embolization coil placed inside the aneurysm. It is made of uncoated metal [e.g., nickel-titanium alloy (Nitinol)] and self-expands after it is delivered to the site of implantation and released (e.g., from a dedicated delivery instrument). Disposable devices associated with implantation may be included.
Who makes Surpass Streamline?
Surpass Streamline is made by Stryker Corporation. It is listed under flow diverters in our device library.
What sizes does Surpass Streamline come in?
Sizes listed for Surpass Streamline: Length: 15–50 mm; Lumen/Inner Diameter: 3–5 mm. Confirm availability with the manufacturer's instructions for use.
Is Surpass Streamline MRI safe?
The FDA device database lists Surpass Streamline as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Surpass Streamline FDA cleared?
Surpass Streamline is registered in the FDA's Global Unique Device Identification Database (GUDID).
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.