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FDA 510(k)

U2 Total Knee System-PF+

K-Number: K221705 · 2023-02-28

ApplicantUnited Orthopedic Corporation
Decision Date2023-02-28
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

U2 Total Knee System-PF+ is a medical device manufactured by United Orthopedic Corporation. It received FDA 510(k) clearance on 2023-02-28 under approval number K221705. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U2 Total Knee System-PF+?

U2 Total Knee System-PF+ is a medical device that received FDA 510(k) clearance on 2023-02-28. It is manufactured by United Orthopedic Corporation. The 510(k) number is K221705.

When was U2 Total Knee System-PF+ approved by the FDA?

U2 Total Knee System-PF+ received FDA 510(k) clearance on 2023-02-28, under approval number K221705.

What company makes U2 Total Knee System-PF+?

U2 Total Knee System-PF+ is manufactured by United Orthopedic Corporation.

What is the FDA product code for U2 Total Knee System-PF+?

The FDA product code for U2 Total Knee System-PF+ is MBH.

Related Clinical Trials

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Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026)

Other Devices by United Orthopedic Corporation

K152430All Poly Tibial Component K152439U2 Bipolar Implant and 22mm Femoral Head K152530UCP Stem K172251UTS Stem K170089U-Motion II Acetabular System— Additional sizes K163441Locking Cage, Full XPE Cup

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Related Devices (Code: MBH)

K162256Klassic Femur, Porous, Klassic Tibial Baseplate, PorousTotal Joint Orthopedics, Inc. K153657Vanguard XP Knee SystemBiomet, Inc. K153776Optetrak One Logic Femoral ComponentsExactech, Inc. K153586Arthrex iBalance TKA SystemArthrex, Inc. K172634Triathlon® X3® UHMWPE Tibial Inserts and Patellar ComponentsHowmedica Osteonics Corp. A.K.A. Stryker Orthopaedics K171365Arthrex Knee SystemsArthrex, 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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