Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell, MetaFix™ Hip System, TriFit™ CF and TS Hip Systems, TaperFit™ Hip System, Revival™ Modular Hip System, MiniHip™, Trinity™ Dual Mobility, MobiliT, BiPolar-i, OMNI MOD™ Hip System, OMNI K1 and K2 Hip Systems, OMNI Bipolar Heads, Corin Biolox Delta Ceramic Heads, OMNI Delta Ceramic Heads

FDA 510(k) K201657 · Corin, Ltd.

Substantially Equivalent

510(k) numberK201657

Submission

Device name
Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell, MetaFix™ Hip System, TriFit™ CF and TS Hip Systems, TaperFit™ Hip System, Revival™ Modular Hip System, MiniHip™, Trinity™ Dual Mobility, MobiliT, BiPolar-i, OMNI MOD™ Hip System, OMNI K1 and K2 Hip Systems, OMNI Bipolar Heads, Corin Biolox Delta Ceramic Heads, OMNI Delta Ceramic Heads
Applicant
Corin, Ltd.
Raynham, MA, US
Received
June 18, 2020
Decision date
July 28, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

Other 510(k)s with product code LZO

510(k)DeviceApplicantDecision
K253948Momentum Acetabular Cup SystemLZO · Traditional United Orthopedic Corporation09/02/2026SE
K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)LZO · Traditional Waldemar Link GmbH & Co. KG07/06/2026SE
K260831Z1 Hip SystemLZO · Traditional Zimmer, Inc.06/16/2026SE
K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemLZO · Traditional Zimmer, Inc.04/27/2026SE
K260037implantcast Packaging System UpdateLZO · Traditional Implantcast GmbH03/30/2026SE
K252401implaFit® short stemsLZO · Traditional Implantcast GmbH03/12/2026SE
K253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)LZO · Traditional Maxx Orthopedics, Inc.01/15/2026SE
K250450Coated hip implantsLZO · Traditional Medacta International S.A.09/19/2025SE
K243021Longboard Revision Hip StemLZO · Traditional Signature Orthopaedics Pty, Ltd.08/07/2025SE
K251906Z1 Hip SystemLZO · Special Zimmer, Inc.07/18/2025SE

More from Zimmer, Inc.

510(k)DeviceDecision
K261576Icona Hip StemMEH · Traditional 08/10/2026SE
K200888OMNIBotics Knee SystemOLO · Traditional 06/27/2020SE

Questions and answers

When was Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell, MetaFix™ Hip System, TriFit™ CF and TS Hip Systems, TaperFit™ Hip System, Revival™ Modular Hip System, MiniHip™, Trinity™ Dual Mobility, MobiliT, BiPolar-i, OMNI MOD™ Hip System, OMNI K1 and K2 Hip Systems, OMNI Bipolar Heads, Corin Biolox Delta Ceramic Heads, OMNI Delta Ceramic Heads cleared by the FDA?

Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell, MetaFix™ Hip System, TriFit™ CF and TS Hip Systems, TaperFit™ Hip System, Revival™ Modular Hip System, MiniHip™, Trinity™ Dual Mobility, MobiliT, BiPolar-i, OMNI MOD™ Hip System, OMNI K1 and K2 Hip Systems, OMNI Bipolar Heads, Corin Biolox Delta Ceramic Heads, OMNI Delta Ceramic Heads (K201657) received a 510(k) decision of Substantially Equivalent on July 28, 2021, 405 days after the submission was received.

What is the product code of K201657?

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