WOLVERINE Cutting Balloon Dilatation Device 2.75 X 15 | REF H74939403152750

The Boston Scientific WOLVERINE Cutting Balloon Dilatation Device (REF H74939403152750) is a 2.75 mm x 15 mm coronary balloon catheter engineered for controlled dilatation of coronary lesions. It combines a non-compliant balloon platform with longitudinally mounted microsurgical atherotomes designed to score the lesion during inflation, supporting predictable luminal expansion in select coronary interventions.

Key Features
Non-compliant balloon platform with a nominal diameter of 2.75 mm and a working length of 15 mm.
Three to four longitudinally mounted microsurgical atherotomes engineered to create discrete scoring incisions on the lesion surface during inflation.
Rapid exchange (Monorail) catheter design intended to facilitate single-operator handling and device exchanges over a 0.014 in guidewire.
Low-profile balloon and tapered tip configuration intended to support lesion crossing in the coronary vasculature.
Color-coded packaging and hub for quick size identification at the procedural table.

Clinical Applications
Intended for use in interventional cardiology procedures involving balloon dilatation of stenotic coronary lesions.
Commonly considered by clinicians for fibrotic, calcified, or in-stent restenotic lesion preparation prior to definitive therapy.
May be used as part of a lesion preparation strategy ahead of stent deployment, per operator discretion and the device Instructions for Use.
Final clinical suitability, indications, contraindications, warnings, and precautions are determined by the treating physician in accordance with the official Instructions for Use.

Product Information
Brand: Boston Scientific
Product Line: WOLVERINE Cutting Balloon Dilatation Device
Category: Coronary Balloon Catheters
Balloon Diameter: 2.75 mm
Balloon Length: 15 mm
REF / UPN: H74939403152750
Catheter Platform: Rapid exchange (Monorail)
Guidewire Compatibility: 0.014 in (per product line specifications)
Nominal and Rated Burst Pressure: Not specified in the located sources
Minimum Guide Catheter ID: Not specified in the located sources
Sterility: Supplied sterile, single-use device (refer to IFU)
Regulatory Status: Refer to the manufacturer for current regulatory clearances in your region.

REF / UPNH74939403152750
Size2.75 X 15

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