Turbo-Power
Laser atherectomy catheter
Turbo-Power
Laser atherectomy catheter
The Turbo-Power laser atherectomy catheter debulks the lesion in a single step and offers remote automatic rotation for precise directional control. Turbo-Power is the only atherectomy device proven and approved for the treat of ISR.
Clinical image gallery
- Maximal luminal gain¹, ³⁻⁶
Features
Clinical superiority
The only atherectomy device with level 1 clinical data. The Excite** ISR prospective randomized controlled trial, including challenging real-world cases with the longest lesions ever studied, proves superiority over PTA alone.¹
Precise directional control
Remote automatic rotation offers precise directional control allowing the physician to direct treatment into bulk where needed.
Fiber pack eccentric rotation
Increases crossing efficiency in calcified lesions allowing for better deliverability in difficult cases.¹⁰
Specifications
- Model number 423-050
- Catheter diameter
- 2.3 mm
- Vessel diameter
- ≥3.5 mm
- Max guidewire compatibility
- 0.018"
- Sheath compatibility
- 7F
- Max tip outer diameter
- 0.091"
- Max shaft outer diameter
- 0.091"
- Working length
- 120 cm
- Fluence
- 30-60 mJ / mm²
- Repetition rate
- 25-80 Hz
- Model number 420-050
- Catheter diameter
- 2.0 mm
- Vessel diameter
- ≥3.0 mm
- Max guidewire compatibility
- 0.018"
- Sheath compatibility
- 6F
- Max tip outer diameter
- 0.080"
- Max shaft outer diameter
- 0.081"
- Working length
- 150 cm
- Fluence
- 30-60 mJ / mm²
- Repetition rate
- 25-80 Hz
Related products
- The only PMA approved excimer laser system and disposable catheters for the treatment of coronary arterial disease. CVX-300 is also indicated for use in the treatment of peripheral arterial disease. Photoablation is the use of light to break down, vaporize and remove matter. The CVX-300 excimer laser system facilitates photoablation via a variety of Philips laser catheters to remove binding arterial plaques.
- Philips Laser System —Nexcimer— photoablates a wide spectrum of morphologies. Philips laser catheters are indicated in many vessel types and is the only laser system available for lead removal. Powered by a common 100-240V electrical outlet, the system warms up in less than 30 seconds for an easy and fast set-up.
- The Phoenix atherectomy system combines the benefits of existing atherectomy systems to deliver a unique atherectomy option to help physicians tailor the treatment approach for each patient.¹ It cuts, captures, and clears diseased tissue with one insertion. Phoenix treats a broad range of tissue types, from soft plaque to calcified arteries, and can be used for lesions above and below the knee.²,³
Disclaimer
1. Dippel et al. Randomized Controlled Study of Excimer Laser Atherectomy for Treatment of Femoropopliteal In-stent Restenosis: Initial EXCITE ISR Results (2015). JACC 8(1): 92-101.
2. Saxon et al (2013). Heparin bonded, expanded polytetrafluoroethylene lined stent graft in the treatment of femoropopliteal artery disease. JVIR; 24(2).
3. McKinsey J, Zellar T, Rocha-Singh K, et al. Lower Extremity Revascularization Using Directional Atherectomy: 12-Moth Prospective Results of the DEFINITIVE LE Study, JACC Cardiovasc Interv 7 (2014) pp. 923-933.
4. Maehara A, et al. JETSTREAM Atherectomy System can remove superficial calcium in severely calcified peripheral arteries. Abstract Poster, ISET Jan 2013.
5. Babaev A, et al. Tissue Removal Assessment with Ultrasound of the SFA and Popliteal Study (TRUTH): Orbital Atherectomy Acute Date and Intravascular Ultrasound Analysis. JACC Vol 64/11/Suppl B, TCT-131.
6. Maximal luminal gain defined as 50% or greater stenosis reduction.
7. Spectranetics Benchmark Study, unpublished data available upon request. Coll Cardio. 2004;43:1959-1963.
8. Data on file D040242-00
9. Data on file ECO031891
*When comparing 7F Turbo-Power to 2.0 Turbo-Elite. Greater than 10% luminal gain when comparing 6F Turbo- Power to 2.0 Turbo-Elite.
**Excite ISR studied the safety and efficacy of Turbo-Tandem plus PTA and PTA alone. Turbo-Power is substantially equivalent to Turbo-Tandem.
Product availability is subject to country regulatory clearance. Please contact your local sales representative to check the availability in your country.
Always read the label and follow the directions for use.
Philips medical devices should only be used by physicians and teams trained in interventional techniques, including training in the use of this device.
Philips reserves the right to change product specifications without prior notification.
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