Auryon Atherectomy Catheters

FDA 510(k) K220116 · Eximo Medical, Ltd.

Substantially Equivalent

510(k) numberK220116

Submission

Device name
Auryon Atherectomy Catheters
Applicant
Eximo Medical, Ltd.
Rehovot, IL
Received
January 14, 2022
Decision date
September 26, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 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

Other 510(k)s with product code MCW

510(k)DeviceApplicantDecision
K260244Auryon Atherectomy SystemMCW · Traditional Eximo Medical04/10/2026SE
K250723FreedomFlow™ Orbital Circumferential Atherectomy System (H6005/ 4Fr 3-Sphere…MCW · Special Cardio Flow Inc.,04/25/2025SE
K250385Turbo-Elite Laser Atherectomy CatheterMCW · Special Spectranetics03/13/2025SE
K242757Rotarex Atherectomy SystemMCW · Special Bard Peripheral Vascular, Inc.01/30/2025SE
K242947FreedomFlow™ Orbital Circumferential Atherectomy SystemMCW · Special Cardio Flow Inc.,11/05/2024SE
K241553Auryon Atherectomy Catheter 1.7mm; Auryon Atherectomy Catheter 1.7mm, Hydrophilic CoatingMCW · Special Eximo Medical, Ltd.06/27/2024SE
K233483FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)MCW · Special Cardio Flow Inc.,02/15/2024SE
K233668Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic Coating (EXM-4010-H000), Auryon…MCW · Special Eximo Medical, Ltd.12/15/2023SE
K231538FreedomFlow Orbital Circumferential Atherectomy SystemMCW · Traditional Cardio Flow Inc.,09/27/2023SE
K230709Auryon Atherectomy SystemMCW · Special Eximo Medical, Ltd.06/09/2023SE

More from Eximo Medical, Ltd.

510(k)DeviceDecision
K260244Auryon Atherectomy SystemMCW · Traditional 04/10/2026SE
K241553Auryon Atherectomy Catheter 1.7mm; Auryon Atherectomy Catheter 1.7mm, Hydrophilic CoatingMCW · Special 06/27/2024SE
K233668Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic Coating (EXM-4010-H000), Auryon…MCW · Special 12/15/2023SE
K230709Auryon Atherectomy SystemMCW · Special 06/09/2023SE
K221077Auryon Atherectomy SystemMCW · Traditional 06/09/2022SE
K202835Auryon Atherectomy SystemMCW · Special 12/02/2020SE
K181642B-Laser Atherectomy SystemMCW · Traditional 10/05/2018SE

Questions and answers

When was Auryon Atherectomy Catheters cleared by the FDA?

Auryon Atherectomy Catheters (K220116) received a 510(k) decision of Substantially Equivalent on September 26, 2022, 255 days after the submission was received.

What is the product code of K220116?

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