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FDA 510(k)

Phoenix Atherectomy System

K-Number: K182972 · 2018-12-20

ApplicantVolcano Atheromed, Inc.
Decision Date2018-12-20
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Phoenix Atherectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Volcano Atheromed, Inc.. It received FDA 510(k) clearance on 2018-12-20 under 510(k) number K182972. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Phoenix Atherectomy System?

Phoenix Atherectomy System is a medical device that received FDA 510(k) clearance on 2018-12-20. The listed applicant is Volcano Atheromed, Inc.. The 510(k) number is K182972.

When did Phoenix Atherectomy System receive FDA 510(k) clearance?

Phoenix Atherectomy System received FDA 510(k) clearance on 2018-12-20, under 510(k) number K182972.

Who is the listed applicant for Phoenix Atherectomy System?

The FDA 510(k) record lists Volcano Atheromed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Phoenix Atherectomy System?

The FDA product code for Phoenix Atherectomy System is MCW.

Other records listing Volcano Atheromed, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K2115182.4mm X 130cm Phoenix Deflecting Atherectomy System, 1.5mm X 149cm Phoenix Atherectomy SystemK193197QuickClear Mechanical Thrombectomy SystemK181877Phoenix 2.4mm Atherectomy Plus SystemK1723861.8mm X 149cm Phoenix Atherectomy System, 2.2mm X 149cm Phoenix Atherectomy System, 2.4mm X 130cm Phoenix Atherectomy System

Related Devices (Code: MCW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260244Auryon Atherectomy SystemEximo MedicalK250723FreedomFlow™ Orbital Circumferential Atherectomy System (H6005/ 4Fr 3-Sphere Configuration)Cardio Flow Inc.,K250385Turbo-Elite Laser Atherectomy CatheterSpectraneticsK242757Rotarex Atherectomy SystemBard Peripheral Vascular, Inc.K242947FreedomFlow™ Orbital Circumferential Atherectomy SystemCardio Flow Inc.,K241553Auryon Atherectomy Catheter 1.7mm; Auryon Atherectomy Catheter 1.7mm, Hydrophilic CoatingEximo Medical, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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