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SpiderFX® Embolic Protection Device

Filter the Risk

The SpiderFX® Embolic Protection Device allows the use of any 0.014" - 0.018" guidewire for initial lesion cross and SpiderFX delivery catheter placement. The SpiderFX filter is deployed and recovered through a dual-ended and low-profile catheter compatible with a guide catheter/sheath minimum ID of 0.066" (typically a 6F guide catheter or 5F access/long sheath). All components of the device are delivered in a single hoop, with Capture Wire/Nitinol braid Filter pre-loaded in the Delivery End of the SpiderFX Catheter.

Guidewire of Choice
  • The SpiderFX Device allows atraumatic lesion crossing with YOUR CHOICE of any 0.014" or 0.018" guidewire

Superior Trackability
  • 6F guide/5F sheath compatible RX delivery catheter with low 3.2F crossing profile
  • New Flexible Hypotube Connector reduces maximum force required to push filter by an average of 40% compared to SpideRX™
  • 320 cm / 190 cm snapwire and 190 cm wire length options for OTW and RX device interventions

Enhanced Visibility
  • Clearly visible radiopaque markers enable fast filter positioning
  • New direct mouth indicator provides enhanced visualization of filter mouth opening

    FXangio

Excellent Stability

Controlled filter positioning throughout the intervention and during device exchanges:
  • Braided nitinol design provides full wall apposition
  • Capture Wire is designed to rotate and move longitudinally independent of the filter

    FXstability

Size and Indication

SpiderFX offers a broad size range of filter sizes (3 mm - 7 mm) — select the most appropriate filter for SVG Interventions.
Product Spec
         

 

Component Capture Wire Delivery End Recovery End Guide Catheter/Sheath
Model Number Filter Size (mm) Lumen Size (mm) Wire Length OTW/RX (cm) Wire Diameter (inch/mm) Crossing Profile (F) Diameter (F) Minimum ID (inch)
SPD2-US-030-190 3 3.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-030-320 3 3.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-040-190 4 3.1-4.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-040-320 4 3.1-4.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-050-190 5 4.1-5.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-050-320 5 4.1-5.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-060-190 6 4.5-6.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-060-320 6 4.5-6.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-070-190 7 5.5-6.0 SVG
5.5 - 7.0 Carotid		 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-070-320 7 5.5-6.0 SVG
5.5 - 7.0 Carotid		 320/190 0.014/0.36 3.2 4.2 0.066

 

SVG Indication: 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 to 6.0 mm. The safety and effectiveness of this device as an embolic protection system has not been established in the cerebral and peripheral vasculature.
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device.