28 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·OSTEOTIM BGS
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS Total Knee System
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 325 PACEMAKER SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 325 PACEMAKER SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 300 PACEMAKER MAESTRO
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 333 PACEMAKER SYSTEM
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·CDS II (SODIUM CHONDROITIN SULFATE)
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR AND DNA EXTENSION KIT
Mitral Valve Repair Devices
FDA Pre-Market Approval
FDA Class 3
·MITRACLIP NT CLIP DELIVERY SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·Valiant Thoracic Stent Graft with the Captiva Delivery System
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·Endurant Stent Graft System, Endurant II Stent Graft System, Endurant IIs Stent Graft System
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 333 PACEMAKER INTRO. 3 NEW MODELS
Mitral Valve Repair Devices
FDA Pre-Market Approval
FDA Class 3
·MitraClip G4 System
Mitral Valve Repair Devices
FDA Pre-Market Approval
FDA Class 3
·MitraClip G4 Clip Delivery System; MitraClip G5 Delivery System
Tricuspid Valve Repair Device, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·TriClip G4 Delivery System;TriClip G5 Delivery System
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis (for Two-Level)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis (one-level indications)