12 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·September 3, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL·Product code MAI·September 3, 2019
M2A 38MM MOD HD -6MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 29, 2014
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 8, 2013
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·March 14, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·March 14, 2019
GRYPHON BR ANCHOR W/ PROKNOT TECHNOLOGY
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MAI·March 16, 2017
GRYPHON P BR DS ANCHOR W/ORTHOCORD
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MAI·March 16, 2017
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·December 13, 2018
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL·Product code MAI·October 22, 2018
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 5, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 5, 2019