751 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·PRESTIGE LP Cervical Disc
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCADE VASCULAR CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·CORDIS EXOSEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PROSTAR XL 10F PERCUTANEOUS VASCULAR SURGICAL SYSTEM
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
·IN MOTION LUMBAR ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·ProDisc-C Total Disc Replacement
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL® Vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PROSEALING DEVICE (MODEL 1010), DIAGNOSTIC DUETT PRO SEALING DEVICE (MODEL 2210), AND D-STAT FLOWABLE HEMOSTAT...
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL ON-SITE PRECISION CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE AT 6F & PROGLIDE SUTURE-MEDICATED CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DIAGNOSTIC DUETT
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX ACE 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
·VASCULAR SOLUTIONS DUETT SEALING 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
·ANGIO-SEAL Vascular Closure Devices
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·M6-C Artificial Cervical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc L
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·QUICKSEAL SURESHOT ARTERIAL CLOSURE SYSTEM