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Results for “EXCIA L”

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36 devices foundsorted by relevance

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  • Excia® L NK996K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NC435T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK605T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK990K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK994K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK604T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK991K

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NC437T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK598T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NC432T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK608T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK603T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia® L NK600T

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:II

  • Excia Total Hip System Lateral Offset

    Aesculap, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Excia Total Hip System

    Aesculap Implant Systems, LLC,FDA registration: United States Group of variants
    Active Regimes: 510(k) Registry: 510(k) Class:II

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