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Results for “PROSPACE”

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290 devices foundsorted by relevance

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  • Prospace® SN009P

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    Withdrawn Registry: GUDID Class:II

  • ProSpace™ DBM Paste (Syringe) ME911

    Xtant Medical Holdings, Inc.,FDA registration: United States
    None Registry: GUDID Class:II

  • ProSpace™ DBM Paste (Syringe) ME913

    Xtant Medical Holdings, Inc.,FDA registration: United States
    None Registry: GUDID Class:II

  • Prospace® SJ288P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ235P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ238P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN192P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ236P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN041P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO433P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN125P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO432P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN058P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN188P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN183P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO159P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN137P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® Xp SO452P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SJ252P

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    Withdrawn Registry: GUDID Class:II

  • Prospace® SN170P

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

Showing 161-180 of 290