3,285 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIOSEAL VASCULAR CLOSURE DEVICE
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCADE VASCULAR CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (VASCULAR HEMOSTASIS DEVICE)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR SPINE MOBI-C CERVICAL DISC PROSTHESIS (TWO LEVEL INDICATION)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·STARCLOSE SE VASCULAR CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PRO SEALING DEVICE, MODEL 1010
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·StarClose SE Vascular Closure System
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MANTA Vascular Closure Device, 14F, MANTA Vascular Closure Device, 18F, MANTA 8F Depth Locator, MANTA 14F Depth Locator
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·PRODISC-L TOTAL DISC REPLACEMENT
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·PRESTIGE LP Cervical Disc
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE PROGLIDE SUTURE MEDIATED CLOSURE DEVICE, PERCLOSE AT 6F SUTURE MEDIATED CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C Cervical Disc Prosthesis (Two Level)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (TWO-LEVEL INDICATION)