15 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SPINE CRAFT
FDA Adverse Event
Malfunction
·SPINE CRAFT, LLC·Product code HWX·March 12, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·September 22, 2015
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·October 4, 2018
APEX SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·October 19, 2020
VELOX ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code KWQ·June 22, 2020
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·November 22, 2021
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·March 24, 2017
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·September 13, 2018
APEX SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·August 5, 2016
APEX SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·August 9, 2017
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·May 10, 2016
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code NKB·March 26, 2020
APEX SPINE SYSTEM
FDA Adverse Event
Injury
·SPINECRAFT·Product code NKB·October 18, 2013
ASTRA SPINE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code LXH·March 30, 2026
VELOX ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·SPINECRAFT·Product code KWQ·November 13, 2015