Cleared Traditional

K243359 - MagDI System (MAG-02, DS-01) (FDA 510(k) Clearance)

Feb 2025
Decision
122d
Days
Class 2
Risk

K243359 is an FDA 510(k) clearance for the MagDI System (MAG-02, DS-01). This device is classified as a Magnetic Compression Anastomosis System (Class II - Special Controls, product code SAH).

Submitted by Gt Metabolic Solutions, Inc. (San Jose, US). The FDA issued a Cleared decision on February 28, 2025, 122 days after receiving the submission on October 29, 2024.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4816. A Magnetic Compression Anastomosis System Is A Surgical Device Used For The Creation Of Anastomoses In Minimally Invasive And Laparoscopic Surgery In The Gastrointestinal Tract. The System Is Comprised Of Magnet Devices And May Involve A Delivery System. Compression And Necrosis Of Tissue Between Magnet Devices Is Created By Polar Attraction Of The Magnet Devices With Healing Of Tissue Around The Devices. Once The Anastomosis Is Formed, The Magnet Devices Are Expelled Naturally. This Classification Does Not Include Devices Intended For Weight Loss Or Metabolic Disease Treatment.

Submission Details

510(k) Number K243359 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 29, 2024
Decision Date February 28, 2025
Days to Decision 122 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code SAH - Magnetic Compression Anastomosis System
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4816
Definition A Magnetic Compression Anastomosis System Is A Surgical Device Used For The Creation Of Anastomoses In Minimally Invasive And Laparoscopic Surgery In The Gastrointestinal Tract. The System Is Comprised Of Magnet Devices And May Involve A Delivery System. Compression And Necrosis Of Tissue Between Magnet Devices Is Created By Polar Attraction Of The Magnet Devices With Healing Of Tissue Around The Devices. Once The Anastomosis Is Formed, The Magnet Devices Are Expelled Naturally. This Classification Does Not Include Devices Intended For Weight Loss Or Metabolic Disease Treatment