1,538 results · 40ms · Sources: EU EUDAMED, US FDA

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY THREADED FUSION CAGE (TFC)(TM) WITH INSTRUMENTATION

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY TFC DEVICE WITH INSTRUMENTATION (20MM)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY TFC DEVICE WITH INSTRUMENTATION

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY THREADED FUSION CAGE (TFC)(TM) WITH INSTRUMENTATION

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX THREADED FUSION DEVICE, INTER FIX RP THREADED FUSION DEVICE AND LT-CAGE LUMBAR TAPERED FUSION DEVICE

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

FDA Pre-Market Approval
FDA Class 2 ·DIMENSION TPSA FLEX REAGENT CARTRIDGE

Platelet And Plasma Separator For Bone Graft Handling

FDA classification
FDA Class 2 ·Platelet And Plasma Separator For Bone Graft Handling

Device, Mixing And Weighing, Semi-Automated

FDA classification
FDA Class 2 ·Device, Mixing And Weighing, Semi-Automated

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Dental Amalgam

FDA classification
FDA Class 2 ·Dental Amalgam

Active Implantable Bone Conduction Hearing System

FDA classification
FDA Class 2 ·Active Implantable Bone Conduction Hearing System

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535