2,531 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·ACTIVL ARTIFICIAL DISC
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·M6-C Artificial Cervical Disc
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·Spectranetics Laser Sheath (SLS) II and GlideLight Laser Sheath
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Prestige LP Cervical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C Cervical Disc Prosthesis (One Level)
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATH II PRODUCTS
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Simplify Disc
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATHS
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANTICS SLS II LASER SHEATH
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C Cervical Disc Prosthesis
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
·Simplify® Cervical Artificial Disc (2 Level)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (ONE LEVEL)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Simplify® Cervical Artificial Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROTHESIS
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·activL Artifical Disc
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C® Cervical Disc Prosthesis
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS/GlideLight
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS SPECTRANETICS LASER SHEATHS