24 results
·
44ms
·
Sources: EU EUDAMED, US FDA
A-CIFT SoloFuse
FDA 510(k)
FDA Class 2
·Orthopedic
Catheter, Percutaneous
FDA classification
FDA Class 2
·Catheter, Percutaneous
Intervertebral Fusion Device With Integrated Fixation, Cervical
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Cervical
Powered Laser Surgical Instrument
FDA classification
FDA Class 2
·Powered Laser Surgical Instrument