MMX — Device, Percutaneous Retrieval Class II

FDA Device Classification

Classification Details

Product Code
MMX
Device Class
Class II
Regulation Number
870.5150
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K242776limflowLimFlow V-CeiverFebruary 14, 2025
K241259medtronicAmplatz Goose Neck Snare KitJune 3, 2024
K232443argon medical devicesSingle-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitSeptember 7, 2023
K222254cook incorporatedGunther Tulip Vena Cava Filter Retrieval SetMay 16, 2023
K222083limflowLimFlow V-CeiverAugust 9, 2022
K212988onocor vascularONO Retrieval DeviceMay 23, 2022
K213494abbott medicalAveir Retrieval CatheterApril 1, 2022
K200963argon medical devicesHalo Single-Loop Microsnare KitJanuary 5, 2021
K200268argon medical devicesHalo™ Single-Loop Snare KitJune 3, 2020
K193507merit medical systemsMerit ONE Snare SystemJanuary 17, 2020
K191758argon medical devicesSingle-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitDecember 17, 2019
K181757cook incorporatedGünther Tulip® Vena Cava Filter Retrieval SetNovember 6, 2018
K170987avantec vascular corporationCaptus Vascular Retrieval SystemAugust 28, 2017
K163307vascular solutionsExpro Elite Snare, Sympro Elite SnareMarch 8, 2017
K160593cook incorporatedIndy OTW Vascular RetrieverSeptember 2, 2016
K152136c.r. bardRecovery Cone Removal SystemFebruary 18, 2016
K152560neometricsBard Snare Retrieval KitOctober 23, 2015
K151497merit medical systemsEN Snare Endovascular Snare SystemJuly 1, 2015
K142265merit medical systemsONE Snare Endovascular Microsnare SystemNovember 13, 2014
K133681volcano corporationCRUX SNARE FILTER RETRIEVAL SETJanuary 30, 2014