24 results
·
42ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO BONE GRAFT WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
Electrocardiograph
FDA classification
FDA Class 2
·Electrocardiograph
Appliance, Fixation, Spinal Intervertebral Body
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Intervertebral Body
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar