Atlas FDA

MagDI System

FDA 510(k) clearance DEN240013 · decided 2024-07-02

Clearance details

K-number
DEN240013
Device name
MagDI System
Applicant
Gt Metabolic Solutions, Inc.
Decision
Unknown
Date received
2024-03-26
Decision date
2024-07-02
Days to decision
98 days
Clearance type
Post-NSE
Product code
SAH
Device class
2
Regulation number
878.4816
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
San Jose, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
GT Metabolic MagDI System (MAG-01, MAG-02, DS-01) (K253102)Gt Metabolic Solutions, Inc.2026-06-04
Self-Forming Magnet (Flexagon Plus OTOLoc) (K253550)GI Windows, Inc.2026-01-09
Self-Forming Magnet (Flexagon Plus OTOLoc) (K250541)GI Windows, Inc.2025-08-01
Self-Forming Magnet (Flexagon) (K243482)GI Windows, Inc.2025-06-11
MagDI System (MAG-02, DS-01) (K243359)Gt Metabolic Solutions, Inc.2025-02-28
Self-Forming Magnet (FLEX SFM) (K243213)GI Windows, Inc.2025-01-29
MagDI System (MAG-01, DS-01) (K242086)Gt Metabolic Solutions, Inc.2024-10-24

Recalls involving this device

No recalls on record reference this clearance.