8 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TYPE7B
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 27, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 7, 2013
COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, IRVINE·Product code OAD·October 22, 2010
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·October 17, 2025
SPINALPAK ASSEMBLY
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·October 30, 2020
BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·October 25, 2023
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·January 2, 2024
SPINALPAK ASSEMBLY
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·March 22, 2021