The Stryker Surpass Elite Flow Diverter (REF FDE52540) is a self-expanding, braided cobalt-chromium flow-diverting stent designed for endovascular treatment of intracranial aneurysms. With a labeled diameter of 5.25 mm and a working length of 40 mm, this implant is intended to redirect blood flow away from the aneurysm sac and promote stable parent-artery reconstruction.

Key Features
- Braided flow-diverter design engineered for high mesh density and consistent pore coverage across the aneurysm neck.
- Self-expanding cobalt-chromium construction for radial support and vessel wall apposition.
- Radiopaque markers to support fluoroscopic visualization during deployment.
- Labeled dimensions: 5.25 mm diameter x 40 mm length, intended for appropriately sized parent vessels.
- Pre-loaded delivery system compatible with standard neurovascular microcatheter workflows (verify catheter compatibility in the current IFU).

Clinical Applications
- Endovascular flow diversion for intracranial aneurysms in adequately sized parent arteries.
- Reconstruction of the parent vessel across wide-neck, large, or fusiform aneurysm morphologies, where indicated.
- Use as part of a neurointerventional procedure under image guidance by trained specialists.
- Indications, contraindications, vessel-size ranges, and patient selection must follow the current Instructions for Use and applicable local regulatory labeling.

Product Information
- Brand: Stryker
- Product Line: Surpass Elite Flow Diverter
- Category: Flow Diverter / Neurovascular Implant
- REF / UPN: FDE52540
- Diameter: 5.25 mm
- Length: 40 mm
- Material: Cobalt-chromium braided wire construction (per manufacturer literature)
- Delivery System: Pre-loaded on a dedicated delivery wire; microcatheter compatibility per IFU
- Sterility: Supplied sterile for single use
- Storage and Shelf Life: Not specified in the located sources
- Regulatory Status: Availability and approved indications vary by region; confirm with Stryker Neurovascular for the destination market.