576 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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IFA SENSIBAC CINOXACIN
FDA 510(k)
FDA Class 2
·Microbiology
MERCURY DENTAL
FDA 510(k)
FDA Class 2
·Dental
IFA SENSIBAC KANAMYCIN
FDA 510(k)
FDA Class 2
·Microbiology
IFA SENSIBAC PENICILLIN
FDA 510(k)
FDA Class 2
·Microbiology
IFA SENSIBAC STREPTOMYCIN
FDA 510(k)
FDA Class 2
·Microbiology
ARiX RAD Radiographic System
FDA 510(k)
FDA Class 2
·Radiology
IFA SENSIBAC CEFACLOR
FDA 510(k)
FDA Class 2
·Microbiology
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
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·RAY TFC UNITE PRODUCT LINE
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
·LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION CAGE