Tack endovascular system Dissection repair device

Tack endovascular system

Dissection repair device

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The Tack endovascular system is a first-of-its-kind, minimal-metal dissection repair device, purpose-built for precision treatment of post-PTA peripheral arterial dissections to promote healing, improve outcomes, and preserve limbs.

Features
Purpose built
Purpose built

Purpose built

The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Precision repair
Precision repair

Precision repair

Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Preserves options
Preserves options

Preserves options

Leaves behind significantly less metal than stents, preserving vessel integrity, future treatment options and—ultimately—limbs.
Adaptive sizing
Adaptive sizing

Adaptive sizing

Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
  • Purpose built
  • Precision repair
  • Preserves options
  • Adaptive sizing
See all features
Purpose built
Purpose built

Purpose built

The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Precision repair
Precision repair

Precision repair

Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Preserves options
Preserves options

Preserves options

Leaves behind significantly less metal than stents, preserving vessel integrity, future treatment options and—ultimately—limbs.
Adaptive sizing
Adaptive sizing

Adaptive sizing

Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.

Specifications

Tack endovascular system (4F)
Tack endovascular system (4F)
Catalog number
  • 154150041
Catheter length
  • 150 cm
Treatment range (RVD)
  • 1.5-4.5 mm
Tack implant length
  • 6.0 mm
Number of Tacks
  • 4
Tack endovascular system (6F)
Tack endovascular system (6F)
Catheter length
  • 135 cm
Treatment range (RVD)
  • 4.0-8.0 mm
Tack implant length
  • 8.0 mm
Number of Tacks
  • 6
Catalog number
  • 206135061
Tack endovascular system (6F)
Tack endovascular system (6F)
Catheter length
  • 135 cm
Catalog number
  • 156135061
Tack implant length
  • 6.0 mm
Number of Tacks
  • 6
Treatment range (RVD)
  • 3.5-6.0 mm
Tack endovascular system (4F)
Tack endovascular system (4F)
Catalog number
  • 154150041
Catheter length
  • 150 cm
Tack endovascular system (6F)
Tack endovascular system (6F)
Catheter length
  • 135 cm
Treatment range (RVD)
  • 4.0-8.0 mm
See all specifications
Tack endovascular system (4F)
Tack endovascular system (4F)
Catalog number
  • 154150041
Catheter length
  • 150 cm
Treatment range (RVD)
  • 1.5-4.5 mm
Tack implant length
  • 6.0 mm
Number of Tacks
  • 4
Tack endovascular system (6F)
Tack endovascular system (6F)
Catheter length
  • 135 cm
Treatment range (RVD)
  • 4.0-8.0 mm
Tack implant length
  • 8.0 mm
Number of Tacks
  • 6
Catalog number
  • 206135061
Tack endovascular system (6F)
Tack endovascular system (6F)
Catheter length
  • 135 cm
Catalog number
  • 156135061
Tack implant length
  • 6.0 mm
Number of Tacks
  • 6
Treatment range (RVD)
  • 3.5-6.0 mm
Regulatory information
Product risks
  • *Target Limb Salvage: freedom from above ankle target limb amputation; Post-hoc analysis, has not been reviewed by US FDA.
  • 1. Geraghty PJ, Adams GL, Schmidt A, Lichtenberg M, Wissgott C, Armstrong EJ, Hertting K, on behalf of the TOBA II BTK Investigators. "Twelve-month results of Tack-optimized balloon angioplasty using the Tack Endovascular System in below-the-knee arteries (TOBA II BTK)." Journal of Endovascular Therapy 27.4 (2020): 626-636.
  • Intended use:​ The Tack endovascular system (4F, 1.5 mm-4.5 mm) is intended for use in mid/ distal popliteal, tibial and peroneal arteries, ranging in diameter from 1.5 mm to 4.5 mm, for the treatment of post percutaneous transluminal balloon angioplasty (PTA) dissection(s).​ The Tack endovascular system (6F, 3.5-6.0 mm US/ 2.5-6.0 mm EU and 4.0-8.0 mm) is intended for use in the superficial femoral and proximal popliteal arteries ranging in diameter from 3.5 mm to 6.0 mm US/ 2.5 to 6.0 mm EU and 4.0 mm to 8.0 mm for the repair of post percutaneous transluminal balloon angioplasty (PTA) dissection(s). ​
  • ​Contraindications for use:​ The Tack endovascular system is contraindicated for the following: 1. Patients with residual stenosis in the treated segment equal to or greater than 30% after PTA. 2. Tortuous vascular anatomy significant enough to prevent safe introduction and passage of the device. 3. Patients with a known hypersensitivity to nickel titanium alloy (Nitinol). 4. Patients unable to receive standard medication used for interventional procedures such as anticoagulants, contrast agents and antiplatelet therapy.​ Prior to using the Tack endovascular system, please review the instructions for use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use. ​ Tack endovascular system is CE Mark authorized under EC Directive 93/42/EEC.​ ​Tack endovascular system and Tack are registered trademarks of Intact Vascular, Inc. Adaptive sizing is a trademark of Intact Vascular, Inc.​ ​Caution: U.S. Federal law restricts this device to sale by or on the order of a physician.

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