658 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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DURACON UNICOMPARTMENTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM (8 MM ARTICULAR SURFACE)
FDA 510(k)
FDA Class 2
·Orthopedic
P.C.A. MODULAR KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SMITH & NEPHEW INC. UNICOMPARTMENTAL AND BIOCOMPARTMENTAL KNEE SYSTEM INSTRUMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
iBalance UKA Tibial Tray Implant
FDA 510(k)
FDA Class 2
·Orthopedic
CONFORMIS METAL BACKED TIBIAL COMPONENT(MBT)
FDA 510(k)
FDA Class 2
·Orthopedic
KIRSCHNER UNICONDYLAR KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BC Reflex Uni Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
TRIBRID® Unicompartmental Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
ACCIN UNI-KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Persona Partial Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY (TGS UKA) MODULAR TIBIA SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CONFORMIS UNI-CONDYLAR KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX THREADED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·VISTA LORDOTIC INTERBODY FUSION CAGE
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 INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE/RAY TFC UNITE DEVICE