3 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Classification
×
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Lens, Contact (Other Material) - Daily
FDA classification
FDA Class 2
·Lens, Contact (Other Material) - Daily
Device, Neurovascular Embolization
FDA classification
FDA Class 2
·Device, Neurovascular Embolization