4 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
KIPPMED I.V. MANIFOLD
FDA 510(k)
FDA Class 2
·General Hospital
SYNTHES VERTEBRAL SPACER TI
FDA 510(k)
FDA Class 2
·Orthopedic
Spinal Vertebral Body Replacement Device
FDA classification
FDA Class 2
·Spinal Vertebral Body Replacement Device
Set, Administration, Intravascular
FDA classification
FDA Class 2
·Set, Administration, Intravascular