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377 devices foundsorted by relevance

Manufacturer: Orthosoft Inc Clear all

  • ROSA® Knee 20-8020-192-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • ROSA® Knee 20-8020-191-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • ROSA® Knee 20-8020-196-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • ROSA® Knee 20-8020-190-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • ROSA® Robotics 20-8020-013-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • NavitrackER® 20-8087-000-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-150-01

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-142-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-141-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-151-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-150-02

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-150-03

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-140-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-700-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • Signature ONE Software Package 302.4018

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • Signature™ ONE System

    Orthosoft Inc. (d/b/a) Zimmer CAS,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • ROSA® Shoulder System

    Orthosoft Inc. (d/b/a) Zimmer CAS,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • ROSA® Robotics 20-8000-010-33 Open recall

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • ROSA® Shoulder 20-8087-601-00

    Orthosoft Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: GUDID Class:II

  • 20-8000-010-42

    Orthosoft Inc,Canada(FDA applicant)
    Withdrawn Registry: GUDID Class:I

Showing 1-20 of 377