3 results
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43ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Classification
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Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Oximeter, Reprocessed
FDA classification
FDA Class 2
·Oximeter, Reprocessed
Stimulator, Spinal-Cord, Implanted (Pain Relief)
FDA classification
FDA Class 2
·Stimulator, Spinal-Cord, Implanted (Pain Relief)