Conformity Stem Extension Line

FDA 510(k) K242249 · United Orthopedic Corporation

Substantially Equivalent

510(k) numberK242249

Submission

Device name
Conformity Stem Extension Line
Applicant
United Orthopedic Corporation
Hsinchu City, TW
Received
July 31, 2024
Decision date
August 30, 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
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
K253948Momentum Acetabular Cup SystemLZO · Traditional 09/02/2026SE
K252725Stem Extension Line (U2 Total Knee System—PSA Type)JWH · Special 09/25/2025SE
K252303Stem Extension Line (USTAR II System)KRO · Special 08/22/2025SE
K243656U2 Total Knee System – PF+ Patella; USTAR II System– PF+ PatellaMBH · Traditional 07/31/2025SE
K242315Resolve Modular Revision Hip StemMEH · Traditional 05/01/2025SE
K243466Conformity Stem Extension Line, #0LZO · Traditional 01/06/2025SE
K243024Cellbrick Knee SpacerJWH · Traditional 12/20/2024SE
K221705U2 Total Knee System-PF+MBH · Traditional 02/28/2023SE
K221149U-Motion II Acetabular System-Extension lineLZO · Traditional 01/05/2023SE
K221675United U2 femoral head, 22mm delta ceramic headLPH · Special 11/04/2022SE

Questions and answers

When was Conformity Stem Extension Line cleared by the FDA?

Conformity Stem Extension Line (K242249) received a 510(k) decision of Substantially Equivalent on August 30, 2024, 30 days after the submission was received.

What is the product code of K242249?

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.