Revolution External Plating System

FDA 510(k) K233025 · New Standard Device Dba Metalogix

Substantially Equivalent

510(k) numberK233025

Submission

Device name
Revolution External Plating System
Applicant
New Standard Device Dba Metalogix
San Antonio, TX, US
Received
September 22, 2023
Decision date
May 30, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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K252555Medusa Orthopedics Boa External Fixation SystemKTT · Traditional Medusa Orthopedics, LLC11/25/2025SE
K252625The Response Ortho Smart Fixator - Hexapod SystemKTT · Traditional Response Ortho Solutions, LLC11/20/2025SE
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K251862External Fixation Bone DistractorKTT · Traditional Paragon 28, Inc.08/11/2025SE

More from Paragon 28, Inc.

510(k)DeviceDecision
K181630Revolution External Plating SystemKTT · Traditional 05/29/2019SE

Questions and answers

When was Revolution External Plating System cleared by the FDA?

Revolution External Plating System (K233025) received a 510(k) decision of Substantially Equivalent on May 30, 2024, 251 days after the submission was received.

What is the product code of K233025?

The FDA product code is KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, a Class II (moderate risk) device regulated under 21 CFR 888.3030.