6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SEASPINE SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Bone Graft, Cervical
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Cervical
Mesh, Surgical, Polymeric
FDA classification
FDA Class 2
·Mesh, Surgical, Polymeric
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar