BEUDAMED
    10,000 results · 62ms · Sources: EU EUDAMED, US FDA
    Filters FDA Pre Market Approval ×

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    System, Test, Her-2/Neu, Ihc

    FDA Pre-Market Approval
    FDA Class 3 ·HERCEP TEST

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) (R) INTERBODY FUSION SYSTEM

    System, Test, Her-2/Neu, Ihc

    FDA Pre-Market Approval
    FDA Class 3 ·PATWAY HER-2/NEU (4B5) RABBIT MONOCLONAL PRIMARY ANTIBODY

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/L INTERBODY FUSION SYSTEM

    System, Test, Her-2/Neu, Ihc

    FDA Pre-Market Approval
    FDA Class 3 ·HERCEPTEST

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION DEVICE

    Immunohistochemistry Antibody Assay, C-Kit

    FDA Pre-Market Approval
    FDA Class 3 ·PATHWAY ANTI-C-KIT (9.7) PRIMARY ANTIBODY