2,283 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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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/L INTERBODY FUSION SYSTEM
MODIFICATION TO BONE ANCHOR AND KIT (BAK)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Endoform Reconstructive Template - PLGA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Endoform Dental Membrane
FDA 510(k)
FDA Class 2
·Dental
NAVIGUS UNIBODY FIDUCIAL MARKER SYSTEM, MODEL FM-4000
FDA 510(k)
FDA Class 2
·Neurology
ASPIRATION/IRRIGATION CATHETER, MODEL AC-1000
FDA 510(k)
FDA Class 2
·Neurology
BURR HOLE COVER, MODEL XX
FDA 510(k)
FDA Class 2
·Neurology
NAVIGUS TRAJECTORY GUIDE, MODEL TG-XXXX
FDA 510(k)
FDA Class 2
·Neurology
NAVIGUS PASSIVE PROBE, MODEL NP-1000
FDA 510(k)
FDA Class 2
·Neurology
ACTIVE ARRAY CATHETER, MODEL CS-2000
FDA 510(k)
FDA Class 2
·Radiology
NAVIGUS FIDUCIAL MARKER SYSTEM, MODELS FM-1000, FM-2000
FDA 510(k)
FDA Class 2
·Neurology
NAVIGUS II MR
FDA 510(k)
FDA Class 2
·Neurology
NAVIGUS PEEL AWAY INTRODUCER
FDA 510(k)
FDA Class 2
·Neurology
REMOTE INTRODUCER, MODEL PI-1000
FDA 510(k)
FDA Class 2
·Neurology
NAVIGUS PASSIVE HEAD RESTRAINT SYSTEM, MODEL HR-XXX
FDA 510(k)
FDA Class 2
·Neurology
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
·BAK VISTA INTERBODY FUSION CAGE
AXYA MEDICAL INC, BONE ANCHOR SYSTEM AND KIT- (BAK)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery