MedalOne Total Knee System

FDA 510(k) K244039 · Suzhou Microport Orthorecon Co., Ltd.

Substantially Equivalent

510(k) numberK244039

Submission

Device name
MedalOne Total Knee System
Applicant
Suzhou Microport Orthorecon Co., Ltd.
Suzhou, CN
Received
December 30, 2024
Decision date
February 28, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3560
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code JWH

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K260063GSPE SpacerJWH · Traditional The General Hospital Corporation, d/b/a…09/11/2026SE
K262293EVOLUTION MPX™ Total Knee SystemJWH · Traditional Suzhou Microport Orthorecon Co., Ltd.09/10/2026SE
K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and…JWH · Traditional B-One Ortho, Corp.09/08/2026SE
K262130ATTUNE Revision Knee SystemJWH · Traditional Depuy Orthopaedics, Inc.09/04/2026SE
K253961SK Knee SystemJWH · Traditional Just Medical Devices (Tianjin) Co., Ltd.09/01/2026SE
K261563Freedom Total Knee System (E-Poly Tibial Liners)JWH · Traditional Maxx Orthopedics, Inc.08/07/2026SE
K262251ACTIFY™ Total Knee System, ACTIFY™ 3D Total Knee System (ACTIFY MC Tibial Insert)JWH · Special Globus Medical, Inc.07/31/2026SE
K261734Klassic Infection Spacer SystemJWH · Traditional Total Joint Orthopedics, Inc.07/23/2026SE
K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemJWH · Traditional DePuy Ireland UC06/25/2026SE
K261032NovoKnee (SteriKnee)JWH · Special NovoSource04/27/2026SE

More from NovoSource

510(k)DeviceDecision
K262293EVOLUTION MPX™ Total Knee SystemJWH · Traditional 09/10/2026SE

Questions and answers

When was MedalOne Total Knee System cleared by the FDA?

MedalOne Total Knee System (K244039) received a 510(k) decision of Substantially Equivalent on February 28, 2025, 60 days after the submission was received.

What is the product code of K244039?

The FDA product code is JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3560.