118 results
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20ms
·
Sources: EU EUDAMED, US FDA
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BRANTIGEN I/F CAGE(R) USED WITH VSP(R) SPINE PLATES AND PEDICLE SCREWS
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINAL SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE(R) SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·SABER LUMBAR I/F CAGE, JAGUAR LUMBAR I/F CAGE
Spinal Pedicle Screw, Fixation, Appliance System
FDA Pre-Market Approval
FDA Class 3
·LUMBAR I/F CAGE SYSTEM
Acrometrix MSSA Positive Control
FDA UDI
Microgenics Corporation·00884883006379·
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600251·Mand. 2. Molar band W-Fit left 25
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250501·Mand. 2. Molar band W-Fit left 25
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250101·Mand. 2. Molar band W-Fit left 25
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250051·Mand. 2. Molar band W-Fit left 25
PROTEK LOW PROFILE ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·ASTRON PULSAR STENT SYSTEM, PULSAR-18 STENT SYSTEM
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·ATS 3F AORTIC BIOPROSTHESIS