9,245 results
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45ms
·
Sources: EU EUDAMED, US FDA
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Duo Venous Stent System
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY THREADED FUSION CAGE(TFC-TM) DEVICE WITH INSTRUMENTATION
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY THREADED FUSION CAGE (TFC)
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Zilver Vena® Venous Self-Expanding Stent
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) (R) INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY THREADED FUSION CAGE (TFC)(TM) WITH INSTRUMENTATION
FDA Pre-Market Approval
CALCIVIS Imaging System
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE WITH INSTRUMENTATION (20MM)
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE WITH INSTRUMENTATION
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY THREADED FUSION CAGE (TFC)(TM) WITH INSTRUMENTATION
FDA Pre-Market Approval
CALCIVIS Imaging System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Zilver Vena® Venous Self Expanding Stent
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX THREADED FUSION DEVICE, INTER FIX RP THREADED FUSION DEVICE AND LT-CAGE LUMBAR TAPERED FUSION DEVICE
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·ARCTIC FRONT, ARCTIC FRONT ADVANCED, AND FREEZOR MAX CARDIAC CRYOABLATION CATHETERS