69 results
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7ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Wishbone HA
FDA 510(k)
FDA Class 2
·Dental
WishBone Guided Growth System
FDA 510(k)
FDA Class 2
·Orthopedic
WishBone K-Wire System
FDA 510(k)
FDA Class 2
·Orthopedic
WishBone Medical Plate and Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
WishBone Medical Plate and Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
WishBone Medical Plate and Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
Wishbone Medical Plate and Screw System: 3.0mm Screws and 7-Hole Straight Fibula Plate
FDA 510(k)
FDA Class 2
·Orthopedic
LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/L INTERBODY FUSION SYSTEM
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 VISTA INTERBODY FUSION DEVICE
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/CERVICAL (BAK/C) (R) INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION CAGE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC DEVICE INSTRUMENTATION
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
·RAY THREADED FUSION CAGE (TFC)
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE LUMBAR TAPERED FUSION DEVICE (TI AND PEEK)