327 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INTERPORE PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FILLER
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT STRIP BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON 500 BONE GRAFT SUBSTITUTE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUE BLOCKS & GRANULES
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON IMPLANT 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUTE BLOCKS & GRANULES
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·NEUGRAFT
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·MOSAIC PORCINE BIOPROSTHESIS
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Activa, Percept and SenSight Deep Brain Stimulation Therapy System
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·FREESTYLE AORTIC ROOT BIOPROSTHESIS
Stimulator, Electrical, Implanted, For Parkinsonian Symptoms
FDA Pre-Market Approval
FDA Class 3
·Vercise PC and Vercise Gevia Deep Brian Stimulation (DBS) System
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·DEEP BRAIN STIMULATION (DBS) EXTENSION KITS
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·INTERSTIM THERAPY SYSTEM
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·SYNCHROMED(TM) INFUSION SYSTEM