GMK 3D Metal Tibial Tray Extension

FDA 510(k) K253328 · Medacta International S.A.

Substantially Equivalent

510(k) numberK253328

Submission

Device name
GMK 3D Metal Tibial Tray Extension
Applicant
Medacta International S.A.
Castel San Pietro, CH
Received
September 30, 2025
Decision date
February 26, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MBH – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3565
Specialty
Orthopedic
Implant
Yes

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K253239Active-V Total Knee System; World Total Knee SystemMBH · Traditional Signature Orthopaedics Pty, Ltd.12/23/2025SE
K253161Balanced Knee System TriMax Porous Femoral ComponentsMBH · Traditional Ortho Development Corp.12/19/2025SE
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K243656U2 Total Knee System – PF+ Patella; USTAR II System– PF+ PatellaMBH · Traditional United Orthopedic Corporation07/31/2025SE

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Questions and answers

When was GMK 3D Metal Tibial Tray Extension cleared by the FDA?

GMK 3D Metal Tibial Tray Extension (K253328) received a 510(k) decision of Substantially Equivalent on February 26, 2026, 149 days after the submission was received.

What is the product code of K253328?

The FDA product code is MBH – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3565.