Logical Liner; World Liner; World Knee Patella

FDA 510(k) K241690 · Signature Orthopaedics Pty, Ltd.

Substantially Equivalent

510(k) numberK241690

Submission

Device name
Logical Liner; World Liner; World Knee Patella
Applicant
Signature Orthopaedics Pty, Ltd.
Lane Cove West, AU
Received
June 12, 2024
Decision date
August 1, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3353
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code MEH

510(k)DeviceApplicantDecision
K261576Icona Hip StemMEH · Traditional Corin, Ltd.08/10/2026SE
K250375Allure Hip Stem and Intramedullary PlugsMEH · Traditional Waldemar Link GmbH & Co. KG11/05/2025SE
K251166Mfinity Femoral SystemMEH · Traditional Medacta International S.A.06/13/2025SE
K251052Trivicta® Hip StemMEH · Traditional Ortho Development Corp.05/22/2025SE
K242315Resolve Modular Revision Hip StemMEH · Traditional United Orthopedic Corporation05/01/2025SE
K243839Alteon® HA Femoral StemsMEH · Traditional Exactech, Inc.03/10/2025SE
K243162World LinerMEH · Special Signature Orthopaedics Pty, Ltd.11/25/2024SE
K241472Icona Hip StemMEH · Traditional Corin U.S.A. Limited10/03/2024SE
K241875TheRay Collared and Collarless Femoral StemMEH · Traditional Nextstep Arthropedix09/13/2024SE
K233758Trivicta™ Hip StemMEH · Traditional Ortho Development Corp.03/08/2024SE

More from Ortho Development Corp.

510(k)DeviceDecision
K252824Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral HeadJDI · Traditional 03/12/2026SE
K253239Active-V Total Knee System; World Total Knee SystemMBH · Traditional 12/23/2025SE
K251771Cambridge Partial KneeHSX · Traditional 12/16/2025SE
K243021Longboard Revision Hip StemLZO · Traditional 08/07/2025SE
K242674Freedom Posterior Cervical ScrewsNKG · Traditional 05/13/2025SE
K242477Shoulder Soft Tissue AnchorsMBI · Traditional 05/12/2025SE
K243043Origin™ Cemented Hip StemLZO · Traditional 05/02/2025SE
K243029Origin™ TT StemLZO · Traditional 03/11/2025SE
K243162World LinerMEH · Special 11/25/2024SE
K240683Rx Knee SystemJWH · Traditional 09/11/2024SE

Questions and answers

When was Logical Liner; World Liner; World Knee Patella cleared by the FDA?

Logical Liner; World Liner; World Knee Patella (K241690) received a 510(k) decision of Substantially Equivalent on August 1, 2024, 50 days after the submission was received.

What is the product code of K241690?

The FDA product code is MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, a Class II (moderate risk) device regulated under 21 CFR 888.3353.