6 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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IdentiTi Porous Ti Interbody System, Transcend PEEK Interbody System, IdentiTi NanoTec Interbody System, Transcend NanoTec Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
ECG SERIES ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
AMS LARGE PORE POLYPROPHLENE MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
FDA classification
FDA Class 2
·Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Electrocardiograph
FDA classification
FDA Class 2
·Electrocardiograph