4,433 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
FDA Pre-Market Approval
FDA Class 3
·BIRMINGHAM HIP RESURFACING (BHR) SYSTEM
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·CERVICAL-STIM CERVICAL FUSION SYSTEM
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestiege LP Cervical Disc - Two-Level
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NexGen® LPS-Flex / LPS-Mobile Bearing Knee
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE Bone Graft
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C® Cervical Disc Prosthesis Two-Level
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·OSTEOSTIM(R)
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
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·CERVICAL-STIM
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS Total Knee System
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·SpF Implantable Spinal Fusion Stimulators
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·ORTHOPAK(R) BONE GROWTH STIMULATOR
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·SUPARTZ
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
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·Superion Indirect Decompression System (IDS) Kit, Vertiflex Instrument Platform (VIP) Kit
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·EMS SWISS DOLORCLAST
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·SUPARTZ
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY INTEGRATED KNEE REPLACEMENT SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·BRYAN CERVICAL DISC