4 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Lucent; Lucent Ti-Bond Systems
FDA 510(k)
FDA Class 2
·Orthopedic
CAYMAN SCREWS MODEL K2-12-1000-XX, K2-12-1001-XX
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Appliance, Fixation, Spinal Intervertebral Body
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Intervertebral Body