12 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
R3 36MM ID US CRMC LINER 54
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·Product code MJO·March 1, 2012
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·July 21, 2017
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 15, 2011
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·February 7, 2018
MEDTRONIC SURGICAL TISSUE VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·September 23, 2021
MEDTRONIC SURGICAL TISSUE VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·August 9, 2021
MEDTRONIC SURGICAL TISSUE VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·March 29, 2024
RESURFACING FEMORAL HEAD 50MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDI·February 28, 2018
MEDTRONIC SURGICAL TISSUE VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 10, 2023
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·July 17, 2018
MEDTRONIC HALL PROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code LWQ·November 3, 2022