| Capture wire | Delivery end |
Recovery end |
Guide catheter/ sheath |
||||
|---|---|---|---|---|---|---|---|
| Item number | Filter size (mm) |
Target vessel size (mm) | Wire length OTW / RX (cm) | Wire diameter (in / mm) | Crossing profile (Fr) | Diameter (Fr) | Minimum ID (in) |
| SPD2-US-030-320 | 3.0 | 3.0 SVG and carotid | 320 / 190 | 0.014 / 0.36 | 3.2 | 4.2 | 0.066 |
| SPD2-US-040-320 | 4.0 | 3.1–4.0 SVG and carotid | 320 / 190 | 0.014 / 0.36 | 3.2 | 4.2 | 0.066 |
| SPD2-US-050-320 | 5.0 | 4.1–5.0 SVG and carotid 3.0–4.0 lower extremity |
320 / 190 | 0.014 / 0.36 | 3.2 | 4.2 | 0.066 |
| SPD2-US-060-320 | 6.0 | 4.5–6.0 SVG and carotid 3.5–5.0 lower extremity |
320 / 190 | 0.014 / 0.36 | 3.2 | 4.2 | 0.066 |
| SPD2-US-070-320 | 7.0 | 5.5–6.0 SVG 5.5–7.0 carotid 4.5–6.0 lower extremity |
320 / 190 | 0.014 / 0.36 | 3.2 | 4.2 | 0.066 |
Embolic protection devices
SpiderFX™ embolic protection device
The SpiderFX™ embolic protection device can remove debris that dislodges during interventional procedures.
Product details
Lower extremity interventions
The SpiderFX™ embolic protection device is indicated for use as a guidewire and embolic protection system. It can be used to contain and remove embolic material in conjunction with the TurboHawk™ peripheral plaque excision system in the treatment of severely calcified lesions in arteries of the lower extremities. The vessel diameter at the filter basket placement site should be between 3.0 mm and 6.0 mm.
Carotid interventions
The SpiderFX™ embolic protection device is indicated for use as a guidewire and embolic protection system to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in carotid arteries. The diameter of the artery at the site of filter basket placement should be between 3.0 mm and 7.0 mm.
Saphenous vein graft interventions
The SpiderFX™ embolic protection device is indicated for use as an embolic protection system to contain and remove embolic material (thrombus/debris). The device also acts as the guidewire while performing percutaneous transluminal coronary angioplasty or stenting procedures in coronary saphenous vein bypass grafts with reference vessel diameters of 3.0 mm to 6.0 mm. The safety and effectiveness of this device as an embolic protection system has not been established in the cerebral vasculature.
Debris matters
Debris can occur with any endovascular procedure and may lead to complications or poor patient outcomes.
Delivery of choice
The SpiderFX™ device can be delivered over any 0.014" or 0.018" guidewire, allowing physicians to choose their method of delivery for successful placement even in challenging access situations.
Vessel of choice
The SpiderFX™ device has broad indication for use in the carotid arteries, coronary saphenous vein bypass grafts, and lower extremities.
The device has a unique braided nitinol filter that conforms to the vessel wall and maintains full-wall apposition during the intervention. Flow is directed into the filter’s conical design, effectively capturing debris while maintaining blood flow.
A gold tungsten loop around the mouth of the filter and radiopaque markers allows for precise positioning and verification of apposition before proceeding with the intervention.
The capture wire (available in a 320 cm length that can be converted to 190 cm) rotates and moves longitudinally independent of the filter for enhanced stability during the procedure.
Extensive SpiderFX™ portfolio
The SpiderFX™ device is available in a variety of sizes (3.0 mm to 7.0 mm) for optimal fit and apposition in a range of vessels.
SpiderFX™ procedure overview animation (02:17)
Watch an animated procedure overview using the SpiderFX embolic protection device.
