66 results
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16ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VISTA DDD MODEL 942 & 944 AND SOFTWARE MODULE MODEL 2052
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA/VISTA
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS DDD PACEMAKER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK AV DDD/AV II DDDD
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DDD PULSE GENERATOR 674
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VIGOR DDD PACEMAKER SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA PACEMAKER SYSTRM; VIGOR DDD MODEL 950 (MASTER)
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CETA DDD MODEL 1230 PACER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·CHARITE ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·PRODISC -L TOTAL DISC REPLACEMENT DEVICE
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·THORATEC VENTRICULAR ASSIST DEVICE (VAD)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA PACEMAKER SYS; VIGOR DDD MODEL 950
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AUTIMA PACING SYSTEM (META DDD MODEL 1230)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc L Total Disc Replacement
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODEL 6291,2,6 & META DDD MODEL 1230
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE