92 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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S.A.F. ACETABULAR CUP WITH POROUS COATING
FDA 510(k)
FDA Class 3
·Orthopedic
SAMUELSON ACETABULAR CUP
FDA 510(k)
FDA Class 3
·Orthopedic
SAMUELSON SCREWLOC CUP
FDA 510(k)
FDA Class 3
·Orthopedic
CLX ACETABULAR CUP (WAGNER) FOR CEMENTLESS FIXAT.
FDA 510(k)
FDA Class 3
·Orthopedic
SCHUSTER ACETABULAR CUP FOR CEMENT/CEMENTLESS FIX.
FDA 510(k)
FDA Class 3
·Orthopedic
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Deep Brain Stimulation (DBS) External Pulse Generator (EPG), Infinity DBS EPG Base
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Dorsal Root Ganglion (DRG) External Pulse Generator (EPG), Proclaim DRG EPG Base
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Spinal Cord Stimulation (SCS) External Pulse Generator (EPG), Proclaim SCS EPG Base
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·EPi-Sense® Guided Coagulation System and EPi-Sense ST Coagulation System
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI PACING LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI 4965/4968
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI PACING LEADS
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI UNIPOLAR/BIPOLAR LEADS
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI UNIPOLAR/BIOPOLAR LEADS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DISPOSABLE EPG COVER/DISPOSABLE POUCH
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI UNIPOLAR/BIPOLAR LEADS
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE EPI UNIPOLAR/BIPOLAR LEAD
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·EPi-Sense Guided Coagulation System
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·EPi-Sense Guided Coagulation System
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 5441 EPG PLASTIC COVER