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FDA 510(k)

FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)

K-Number: K233483 · 2024-02-15

ApplicantCardio Flow Inc.,
Decision Date2024-02-15
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) is a medical device manufactured by Cardio Flow Inc.,. It received FDA 510(k) clearance on 2024-02-15 under approval number K233483. 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 FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)?

FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) is a medical device that received FDA 510(k) clearance on 2024-02-15. It is manufactured by Cardio Flow Inc.,. The 510(k) number is K233483.

When was FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) approved by the FDA?

FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) received FDA 510(k) clearance on 2024-02-15, under approval number K233483.

What company makes FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)?

FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) is manufactured by Cardio Flow Inc.,.

What is the FDA product code for FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)?

The FDA product code for FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration) is MCW.

Related Clinical Trials

NCT07475091 Standardizing Swallow Pressure Measurements NOT_YET_RECRUITING NCT07308847 Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With the Sphere-360™ Catheter and Affera™ Mapping and Ablation System (Horizon 360) RECRUITING NCT07581977 A Novel Two-Tooth Clip for ESD and EFTR of GIST RECRUITING NCT04229563 Post-Market Registry of AURYON Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease COMPLETED NCT07585968 Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System for the Treatment of Ventricular Tachycardia (Sphere VT) NOT_YET_RECRUITING NCT06858306 SPHERE Per-AF Post-Approval Study ACTIVE_NOT_RECRUITING

Other Devices by Cardio Flow Inc.,

K213834Cardio Flow Peripheral Guide Wire K231538FreedomFlow Orbital Circumferential Atherectomy System K242947FreedomFlow™ Orbital Circumferential Atherectomy System K250723FreedomFlow™ Orbital Circumferential Atherectomy System (H6005/ 4Fr 3-Sphere Configuration)

Related Devices (Code: MCW)

K163264Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox SledAvinger, Inc. K162326Pantheris Catheter, Lightbix HS Imaging Console, Lightbox SledAvinger, Inc. K161361HawkOne Directional Atherectomy SystemMedtronic Vascular, Inc. K160827Pantheris CatheterAvinger, Inc. K153460Pantheris Catheter (8Fr), Pantheris Catheter (7Fr)Avinger, Inc. K172687Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy CathetersSpectranetics, Inc.

Official Source

View on FDA Database →

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

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