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FDA 510(k)

Momentum Acetabular Cup System

K-Number: K253948 · 2026-09-02

ApplicantUnited Orthopedic Corporation
Decision Date2026-09-02
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Momentum Acetabular Cup System is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2026-09-02 under 510(k) number K253948. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Momentum Acetabular Cup System?

Momentum Acetabular Cup System is a medical device that received FDA 510(k) clearance on 2026-09-02. The listed applicant is United Orthopedic Corporation. The 510(k) number is K253948.

When did Momentum Acetabular Cup System receive FDA 510(k) clearance?

Momentum Acetabular Cup System received FDA 510(k) clearance on 2026-09-02, under 510(k) number K253948.

Who is the listed applicant for Momentum Acetabular Cup System?

The FDA 510(k) record lists United Orthopedic Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Momentum Acetabular Cup System?

The FDA product code for Momentum Acetabular Cup System is LZO.

Other records listing United Orthopedic Corporation as applicant

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Related Devices (Code: LZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbHK252401implaFit® short stemsImplantcast GmbHK253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)Maxx Orthopedics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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