FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GT Metabolic MagDI System (MAG-01, MAG-02, DS-01)

K Number: K253102 · Decision Jun 4, 2026
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
7
Applicant Total
4
Review Days
253

Basic Information

Device Name
GT Metabolic MagDI System (MAG-01, MAG-02, DS-01)
K Number
K253102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4816
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gt Metabolic Solutions, Inc.
Date Received
September 24, 2025
Decision Date
June 4, 2026
Product Code
SAH
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
SAH Magnetic Compression Anastomosis System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (SAH), ordered by most recent decision date.

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Other Clearances by Gt Metabolic Solutions, Inc.

K Number Device Name
K243359 MagDI System (MAG-02, DS-01)
K242086 MagDI System (MAG-01, DS-01)
DEN240013 MagDI System