Phoenix 2.4mm X 130cm 7f Deflecting Atherectomy System
The Phoenix 2.4 mm by 130 cm Deflecting Atherectomy System removes plaque from peripheral blood vessels. It is a sterile, single-use system with a catheter and a battery-powered handle. It…
The Phoenix 2.4 mm by 130 cm Deflecting Atherectomy System removes plaque from peripheral blood vessels. It is a sterile, single-use system with a catheter and a battery-powered handle. It is not intended for coronary, carotid, iliac or renal vessels.
The catheter passes over a guidewire and uses a rotating cutter at its front to remove plaque. The handle motor drives the cutter. Removed material travels back through the catheter and handle into a collection reservoir outside the patient. An on/off slider on the handle controls activation.
Guidewire Support
A wire support clip holds the guidewire fixed relative to the handle and prevents guidewire rotation during use. Phoenix catheter models are compatible with 0.014-inch exchange-length guidewires of at least 260 cm.
Who Else Makes It
All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| ATL Technology DG,Ltd. | Dongguan | Guangdong | Contract manufacturer | 14 |
| Quasar Electronics Technology (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 2 |
| Dongguan King Medical Technology Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 14 |
Record
| Listed by | Volcano Atheromed, Inc., United States |
|---|---|
| FDA product code | MCW |
| Device type | Catheter, Peripheral, Atherectomy |
| Device class | Class 2 |
| Regulation | 21 CFR 870.4875 |
| 510(k) | K211518 |
| Record published | 2021-10-26 |
| Record revised | 2025-03-27 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Keep dry; Special storage condition: Keep away from sunlight |
| Sizes | Outer diameter 2.4 mm; length 130 cm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| PD24130K | Outer Diameter 2.4 mm | In distribution |
| PD24130 | Outer Diameter 2.4 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Diamondback Peripheral | Cardiovascular Systems Incorporated | 44 |
| Turbo-Elite™ | Spectranetics Corp. | 24 |
| Stealth | Cardiovascular Systems Incorporated | 20 |
| Zilient | Cardiovascular Systems Incorporated | 16 |
| TurboHawk | Covidien LP | 15 |
| HawkOne | Covidien LP | 14 |
| Turbo-Elite Laser Atherectomy Catheter | Spectranetics Corp. | 12 |
| SilverHawk | Covidien LP | 11 |
| Auryon Atherectomy Catheter | Eximo Medical Ltd | 10 |
| Revolution Peripheral Atherectomy System | Rex Medical | 8 |
| Peripheral RotaLink® Plus | Boston Scientific Corporation | 8 |
| SilverHawkTM | Covidien LP | 8 |
Showing 12 of 102. All products under Catheter, Peripheral, Atherectomy
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K211518 | 2021-06-14 |
| K182972 | 2018-12-20 |
| K181877 | 2018-12-17 |
| K172386 | 2017-08-24 |
| K151145 | 2015-05-26 |
| K143328 | 2014-12-19 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.