The Boston Scientific Peripheral Cutting Balloon (REF M001BP90720B0) is a microsurgical dilatation catheter that combines a non-compliant balloon with longitudinally mounted atherotomes designed to deliver controlled, focal incisions to the lesion during inflation. With a nominal balloon size of 7 mm in diameter and 20 mm in length, this device is intended to support predictable luminal gain in peripheral interventional procedures.
Key Features
- Four longitudinally mounted microsurgical atherotomes for controlled scoring of the lesion
- Non-compliant balloon construction for focused, predictable expansion
- Nominal diameter 7 mm, working length 20 mm
- Over-the-wire catheter platform compatible with standard peripheral guidewires (refer to IFU for specific compatibility)
- Designed to reduce barotrauma compared with conventional plain balloon angioplasty in fibrotic or resistant lesions
- Single-use, sterile, supplied individually packaged
Clinical Applications
- Dilatation of stenoses in the peripheral vasculature as defined by the manufacturer's Instructions for Use
- Treatment of fibrotic, calcified or resistant peripheral lesions where focal scoring may aid controlled dilatation
- Management of in-stent restenosis where indicated by the IFU
- Adjunctive lesion preparation prior to additional endovascular therapy at the operator's discretion
Refer to the official IFU for the complete list of indications, contraindications and warnings.
Product Information
- Brand: Boston Scientific
- Product: Peripheral Cutting Balloon Microsurgical Dilatation Device
- REF / UPN: M001BP90720B0
- Balloon diameter: 7 mm
- Balloon length: 20 mm
- Category: Peripheral Balloon Catheters
- Rated burst pressure: Not specified in the located sources
- Catheter working length: Not specified in the located sources
- Guidewire compatibility: Not specified in the located sources
- Introducer sheath compatibility: Not specified in the located sources
- Sterility: Sterile, single-use
- Packaging: Individually packaged unit
Regulatory status, indications and availability vary by country; confirm local approvals and the current IFU prior to ordering.