344 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Evera MRI DF-I ICD/Evera MRI ICD/ Evera S DR ICD/Evera S VR ICD/ Evera XT DR ICD/ Evera XT VR ICD/ Visia AF MRI DF1 ICD/
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Evera MRI DF-I ICD / Evera MRI ICD/ S DR ICD / S VR ICD / XT DR ICD /XT VR ICD ; Mirro MRI DR ICD / MRI VR ICD; Primo MR
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Evera MRI DF ICD, MRI ICD, S DR ICD, S VR ICD, XT DR ICD, XT VR ICD - Visia AF MRI DFI ICD, AF MRI VR ICD, AF VR ICD
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CAPSURE(R) AND CAPSURE(R)SP LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CAPSURE(R) AND CAPSURE(R) SP PACING LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CARBON TIPPED LEAD MODELS 1085S,1085M,& 1085K
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·SWEET TIP RX STEROID ELUTING LEAD
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·FLEXTEND BIPOLAR, STEROID ELUTING, EXTENDABLE/ RETRACTABLE PACING LEAD
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·THINLINE/FINELINE
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·SUREFIX TM MODEL 5072 LEAD
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·PASSIVE PLUS DX ENDOCARDIAL, STEROID ELUTING, PASSIVE FIXATION PACING LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·PHILOS FAMILY OF PULSE GENERATORS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·ENDOCARDIAL PACEMAKER LEAD W/CARBON TIP
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CARBON TIPPED LEAD ALT.PROD.TRAYS