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SpiderFX™ Embolic Protection Device

The Ultimate in Embolic Protection

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 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 (3 mm - 7 mm) — select the most appropriate filter for both Carotid and SVG Interventions
For additional product information please contact your regional sales representative.
The SpiderFX Embolic Protection Device provides distal embolization protection during general vascular use, including peripheral, coronary, and carotid interventions.
Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device.