2.4mm X 127 cm Phoenix Atherectomy Deflecting System

FDA 510(k) K151145 · Volcano Atheromed, Inc.

Substantially Equivalent

510(k) numberK151145

Submission

Device name
2.4mm X 127 cm Phoenix Atherectomy Deflecting System
Applicant
Volcano Atheromed, Inc.
Menlo Park, CA, US
Received
April 29, 2015
Decision date
May 26, 2015
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MCW – Catheter, Peripheral, Atherectomy
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4875
Specialty
Cardiovascular

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K233668Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic Coating (EXM-4010-H000), Auryon…MCW · Special Eximo Medical, Ltd.12/15/2023SE
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K230709Auryon Atherectomy SystemMCW · Special Eximo Medical, Ltd.06/09/2023SE

More from Eximo Medical, Ltd.

510(k)DeviceDecision
K2115182.4mm X 130cm Phoenix Deflecting Atherectomy System, 1.5mm X 149cm Phoenix Atherectomy…MCW · Special 06/14/2021SE
K193197QuickClear Mechanical Thrombectomy SystemQEZ · Traditional 04/20/2020SE
K182972Phoenix Atherectomy SystemMCW · Special 12/20/2018SE
K181877Phoenix 2.4mm Atherectomy Plus SystemMCW · Traditional 12/17/2018SE
K1723861.8mm X 149cm Phoenix Atherectomy System, 2.2mm X 149cm Phoenix Atherectomy System…MCW · Special 08/24/2017SE
K1433281.8mm X 149 cm Phoenix Atherectomy Catheter, 2.2mm X 149 cm Phoenix Atherectomy…MCW · Special 12/19/2014SE

Questions and answers

When was 2.4mm X 127 cm Phoenix Atherectomy Deflecting System cleared by the FDA?

2.4mm X 127 cm Phoenix Atherectomy Deflecting System (K151145) received a 510(k) decision of Substantially Equivalent on May 26, 2015, 27 days after the submission was received.

What is the product code of K151145?

The FDA product code is MCW – Catheter, Peripheral, Atherectomy, a Class II (moderate risk) device regulated under 21 CFR 870.4875.