BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    SeaSpine Spacer System NM (Hollywood, Hollywood VI, Pacifica, Redondo, Ventura), Vu a•POD-L NanoMetalene, SeaSpine Vu e•POD System, SeaSpine Vu a•POD Prime NanoMetalene Intervertebral, SeaSpine Shoreline ACS - Anterior Cervical Standalone, SeaSpine Cervical Interbody RT System, SeaSpine Cambria System, SeaSpine Regatta Lateral System, SeaSpine Reef TO/TA System, SeaSpine Reef TH System, SeaSpine Meridian System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILVERSPEED HYDROPHILIC GUIDEWIRE, MODELS 103-0601-300 AND 103-0602-300

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PASS LP SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Orthosis, Spondylolisthesis Spinal Fixation

    FDA classification
    FDA Class 2 ·Orthosis, Spondylolisthesis Spinal Fixation

    Wire, Guide, Catheter

    FDA classification
    FDA Class 2 ·Wire, Guide, Catheter