389 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2000 SYSTEM
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2000
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE DEVICE
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE SYSTEM
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2100 SYSTEM
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2000/2100 1.5 AND 3T
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2000 SYSTEM
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE SYSTEM
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE 2100 SYSTEM
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NEXGEN COMPLETE KNEE SOLUTION/LEGACY KNEE - POSTERIOR STABILIZED (LPS)/LPS-FLEX MOBILE BEARING KNEE
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestige LP (R) Cervical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestige LP (R) Cervical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestige LP® Cervical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestige LP® Cervical Disc
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NexGen© LPSFlex/LPS Mobile Bearing Knee System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Multiple Application Utility (MAU) and Data Management System (DM) LATITUDE Programming System )LPS)
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Arctic Front Advance and Arctic Front Advance Pro
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·FREEZOR CARDIAC CRYOABLATION CATHETER, FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE, FREEZOR MAX SURGICAL CARDIAC C
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Arctic Front and Arctic Front Advance Cardiac CryoAlbation Catheters