3,285 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·THE CLOSER AK 6 FR. SMC DEVICE
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
·MYNXGRIP VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·D-Stat Flowable hemostat
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
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·CLOSER VASCULAR SEALING SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCULAR SOLUTIONS DUETT SEALING DEVICE
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·M6-C Artificial Cervical Disc
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLATFORM AND ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS PLATFORM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Perclose ProGlide Suture-Mediated Closure System
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MynxGrip Vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL ES DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE A-T MONOFILAMENT 6 FR. SUTURE MEDIATED CLOSURE (SMC) SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Simplify® Cervical Artificial Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Simplify Cervical Artificial Disc
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE PROGLIDE SUTURE MEDIATED CLOSURE SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)