4 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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FOCUS Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
REFORM PEDICLE SCREW SYSTEM
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
Orthosis, Spinal Pedicle Fixation
FDA classification
FDA Class 2
·Orthosis, Spinal Pedicle Fixation