840 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex Interlaminar Stabilization Device
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex® Interlaminar Technology
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex® Interlaminar Technology
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex Interlaminar Stabilization Device
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex Interlaminar Technology
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·Paradigm Spine Coflex Interlaminar Stabilization Device
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex® Interlaminar Technology
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Softec HD, Softec I, Softec HD PS, Softec HDO, and Softec HDM IOLs
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Softec HD, Softec I, Softec HD PS, Softec HDO, and Softec HDM IOLs
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Softec HD, Softec I, Softec HD PS, Softec HDO, and Softec HDM IOLs
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·Gel-One
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC MODEL 2090 BURBOT AND SPLAKE PROGRAMMERS
Immunohistochemistry Assay, Antibody, Epidermal Growth Factor Receptor
FDA Pre-Market Approval
FDA Class 3
·DAKOCYTOMATION EGFR PHARMDX KIT
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·ARCTIC FRONT CARDIAC CRYOABLATION SYSTEM: 23MM AND 28MM ARCTIC FRONT CATHETERS, FREEZOR MAX CATHETER, CRYOCONSOLE, MANUA
Stimulator, Autonomic Nerve, Implanted (Depression)
FDA Pre-Market Approval
FDA Class 3
·VNS THERAPY SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SOFTEE HD POSTERIOR CHAMBER INTRAOCULAR LENS (PCIOL)