47 results
·
49ms
·
Sources: EU EUDAMED, US FDA
PROW FUSION
FDA 510(k)
FDA Class 2
·Orthopedic
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970492·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970485·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970553·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970546·
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Powered Laser Surgical Instrument
FDA classification
FDA Class 2
·Powered Laser Surgical Instrument