444 results
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22ms
·
Sources: EU EUDAMED, US FDA
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Roadsaver/CASPER Carotid Stent Device
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Roadsaver/CASPER Carotid Stent Device
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 11, 2025
CASPER 5F
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 24, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 21, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 21, 2025
CASPER 5F
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·April 1, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 28, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 24, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 23, 2025
CASPER 5F
FDA Adverse Event
Injury
·MICROVENTION INC.·Product code NIM·February 22, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 23, 2025
CASPER X 5F
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 22, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code NIM·February 21, 2025
CASPER X
FDA Adverse Event
Injury
·MICROVENTION INC.·Product code NIM·February 22, 2025
MaXcess
FDA UDI
Nuvasive, Inc.·00887517184467·MaXcess Blade, Light Cable Adapter
AMPLITUDE
FDA UDI
AMPLITUDE SAS·03701089500814·Resurfacing Patellar Implant NM Cemented Ø 30 mm
LEONE SPA
FDA UDI
LEONE SPA·08033707080817·THREE-JAW PLIERS CLASSIX
APEX Spine System
FDA UDI
SPINECRAFT, LLC·00193082014765·APEX Ti Poly Screw Dia.10.0, 30mm
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869621151·MOSS VRS Ti rod, Ø5.5x30mm, curved