7,912 results
·
59ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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IRRI-FLO IRRIGATION DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURGITEK CO2 DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURGITEK (R) UROFLOW SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
E.R.C.P. CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STONE BASKET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURGITEK(R) LAPAROSCOPIC CHOLANGIOGRAM KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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
Discs, Elution
FDA Pre-Market Approval
FDA Class 2
·AMIKACIN ELUTION DISK FOR AUTOBAC
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Discs, Elution
FDA Pre-Market Approval
FDA Class 2
·AMIKACIN ELUTION DISK FOR AUTOBAC
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM
Discs, Elution
FDA Pre-Market Approval
FDA Class 2
·AMIKACIN ELUTION DISK FOR AUTOBAC
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