2,699 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LOCK-CAP ONE-STEP F/MATRIX 5.5 TAN
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code NKB·December 18, 2013
LOCK-CAP ONE-STEP F/MATRIX 5.5 TAN
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code NKB·December 18, 2013
MATRIX LOCKING CAP WITHOUT SADDLE
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 5, 2015
7.0MM TI MATRIX POLYAXIAL SCREW 45MM THREAD LENGTH
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 5, 2015
7.0MM TI MATRIX POLYAXIAL SCREW 45MM THREAD LENGTH
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 5, 2015
5.5MM TI MIN INVASIVE CURVED ROD 200MM RADIUS/125MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NKB·March 12, 2013
PEDICSCR PANGEAPOLYAX Ø6 CANN PREASSMBL
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code NKB·February 12, 2013
7.0MM TI MATRIX POLYAXIAL SCREW 50MM THREAD LENGTH
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·January 24, 2017
TI PANGEA(TM) LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·January 19, 2016
6.0MM TI COLLAR
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·October 12, 2015
TI PANGEA(TM) LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·January 19, 2016
6.0MM TI COLLAR
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·October 12, 2015
6.0MM TI COLLAR
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·October 12, 2015
LOCKING DRILL GUIDE FOR EXPANSIONHEAD SCREWS
FDA Adverse Event
Malfunction
·SYNTHES JENNERSVILLE·Product code LXH·March 18, 2013
TI MATRIX LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·September 30, 2013
SYNERGY SPINAL SYSTEM
FDA Adverse Event
Other
·INTERPORE CROSS INTERNATIONAL·Product code KWO·March 12, 2004
SYNERGY SPINAL SYSTEM
FDA Adverse Event
Other
·INTERPORE CROSS INTL.·Product code KWO·February 25, 2004
SYNERGY SPINAL SYSTEM
FDA Adverse Event
Other
·INTERPORE CROSS INTL.·Product code KWO·February 25, 2004
NONE
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code KWO·February 11, 2013
NONE
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code KWO·February 11, 2013