The Stryker Surpass Evolve Flow Diverter (REF FD50015) is a self-expanding, braided flow diverting stent designed for the endovascular treatment of intracranial aneurysms. This 5.00 mm diameter x 15 mm length configuration is pre-loaded on a dedicated delivery system and is intended to divert blood flow away from the aneurysm sac while preserving flow through adjacent perforators and side branches, promoting progressive aneurysm occlusion and parent artery reconstruction.

Key Features
- 64-wire braided construction engineered to provide consistent metal coverage across the device length.
- Cobalt chromium alloy wires for radial strength with platinum wires interwoven for fluoroscopic visibility.
- Self-expanding design enabling controlled deployment and wall apposition in tortuous intracranial anatomy.
- Pre-loaded delivery system intended to streamline preparation and deployment.
- Radiopaque markers at proximal and distal ends to support accurate positioning under fluoroscopy.
- Re-sheathable up to a manufacturer-defined threshold for repositioning prior to full deployment (refer to current IFU).

Clinical Applications
- Endovascular flow diversion for intracranial aneurysms of the internal carotid artery and other indicated cerebral vessels, per the approved IFU in the applicable jurisdiction.
- Treatment of wide-necked, large, or giant aneurysms where conventional coiling or stent-assisted coiling may be suboptimal.
- Reconstruction of diseased parent artery segments as part of a neurointerventional treatment plan.
- Intended for use by physicians trained in interventional neuroradiology and flow diverter deployment techniques.

Product Information
- Brand: Stryker
- Product Line: Surpass Evolve Flow Diverter
- Category: Flow Diverter / Neurovascular Stent
- REF / UPN: FD50015
- Nominal Diameter: 5.00 mm
- Nominal Length: 15 mm
- Material: Cobalt chromium alloy with platinum radiopaque wires
- Construction: 64-wire braided design
- Delivery System: Pre-loaded dedicated delivery system (compatible microcatheter per IFU)
- Sterility: Sterile, single-use device
- Storage: Store per manufacturer instructions
- Regulatory Status: Not specified in the located sources — refer to current manufacturer IFU and regional regulatory documentation prior to use.