Trinity EVO Acetabular Shell

FDA 510(k) K242744 · Corin U.S.A. Limited

Substantially Equivalent

510(k) numberK242744

Submission

Device name
Trinity EVO Acetabular Shell
Applicant
Corin U.S.A. Limited
Tampa, FL, US
Received
September 11, 2024
Decision date
June 5, 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
LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3358
Specialty
Orthopedic
Implant
Yes

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K243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi…LPH · Traditional Nextstep Arthopedix, LLC06/05/2026SE
K251270Taperloc® Complete Hip StemLPH · Traditional Biomet, Inc.05/19/2026SE
K252623G7® Revision Acetabular SystemLPH · Traditional Zimmer, Inc.02/04/2026SE
K251043Mpact 3D Metal Implants Extension – DMLS TechnologyLPH · Traditional Medacta International S.A.01/28/2026SE
K252067Velora Acetabular SystemLPH · Traditional Restor3D, Inc.12/05/2025SE
K252846TaperSet™ Hip SystemLPH · Special Shalby Advanced Technologies, Inc. Dba Consensus…11/20/2025SE
K251833EMPOWR Acetabular® Liner ExtensionLPH · Traditional Encore Medical L.P.11/12/2025SE

More from Encore Medical L.P.

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K241570Unity Total Knee SystemJWH · Traditional 09/23/2024SE
K240875Unity Knee PS-C Tibial InsertJWH · Traditional 06/26/2024SE
K231172ApolloKneeOLO · Traditional 07/26/2023SE
K212069Corin MetaFix™ Hip StemLZO · Traditional 04/07/2022SE
K191831MobiliT CupLZO · Traditional 01/16/2020SE
K191374Revival Modular Hip StemLZO · Traditional 07/22/2019SE
K183114Corin BiPolar-iKWY · Traditional 06/05/2019SE
K183533Unity Total Knee SystemJWH · Traditional 06/04/2019SE

Questions and answers

When was Trinity EVO Acetabular Shell cleared by the FDA?

Trinity EVO Acetabular Shell (K242744) received a 510(k) decision of Substantially Equivalent on June 5, 2025, 267 days after the submission was received.

What is the product code of K242744?

The FDA product code is LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3358.