Product Code: MMX FDA class 2 21 CFR 870.5150

Device, Percutaneous Retrieval

Cardiovascular

The Percutaneous Retrieval Device is a catheter-based instrument used to grasp and remove foreign bodies, emboli, or misplaced devices from within blood vessels or cardiac chambers via a minimally invasive percutaneous approach, avoiding the need for open surgery. Classified as a Class 2 device under 21 CFR 870.5150 within the Cardiovascular specialty, it requires 510(k) premarket notification. It carries no implant or life-sustaining flags.

510(k)s
32
FEI Numbers
36
Registration Numbers
36
Unique Applicants
19
Years Active
23

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Basic Information

Product Code
MMX
Device Class
FDA class 2
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Review Panel
CV
Submission Type
1

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 32 510(k) clearances via K numbers.

K Number Device Name
K242776 LimFlow V-Ceiver
K241259 Amplatz Goose Neck Snare Kit
K232443 Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
K222254 Gunther Tulip Vena Cava Filter Retrieval Set
K222083 LimFlow V-Ceiver
K212988 ONO Retrieval Device
K213494 Aveir Retrieval Catheter
K200963 Halo Single-Loop Microsnare Kit
K200268 Halo™ Single-Loop Snare Kit
K193507 Merit ONE Snare System
K191758 Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
K181757 Günther Tulip® Vena Cava Filter Retrieval Set
K170987 Captus Vascular Retrieval System
K163307 Expro Elite Snare, Sympro Elite Snare
K160593 Indy OTW Vascular Retriever
K152136 Recovery Cone Removal System
K152560 Bard Snare Retrieval Kit
K151497 EN Snare Endovascular Snare System
K142265 ONE Snare Endovascular Microsnare System
K133681 CRUX SNARE FILTER RETRIEVAL SET
K122088 MERIT ONE SNARE SYSTEM
K112185 FOURSNARE VASCULAR RETRIEVAL SNARE
K102484 SEQURE SNARE SYSTEM
K092343 EN SNARE ENDOVASCULAR SNARE SYSTEM
K091563 RECRUIT MICROCATHETER
K071457 MODIFICATION TO RADIUS SNARE
K050926 TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060
K033188 TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050
K022201 RADIUS MICRO SNARE
K021441 RADIUS SNARE
K021606 EN-SNARE ENDOVASCULAR SNARE AND CATHETER
K014109 IN-TIME RETRIEVAL DEVICE

FEI Numbers

This FDA classification entry is associated with 36 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 36 registration numbers. Click on an entry to view related FDA registrations.