4,052 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NFLEX CURV 1SEGM L55 PCU/TAV-ELI
FDA Adverse Event
Injury
·SYNTHES ELMIRA·Product code NQP·January 12, 2014
TI STENOFIX INTERSPINOUS IMPLANT 12MM-STERILE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code MNI·March 16, 2023
TI STENOFIX INTERSPINOUS IMPLANT 8MM-STERILE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code MNI·October 31, 2022
1030489-2016-03607
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NQP·December 30, 2016
DYNESYS LIS, STABILIZING CORD, 100
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·October 11, 2016
DYNESYS DTL SPACER CUTTER
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NQP·September 18, 2015
DYNESYS FUSION UNIVERSAL SPACER 6-45
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·September 1, 2015
DYNESYS L.I.S. FUSION CORD 100
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·September 1, 2015
ROD
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code NQP·January 13, 2012
DYNESYS HA PEDICLE+SET SCREW 6.0X45
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·March 29, 2012
DYNESYS IMPLANT GENERIC
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·March 13, 2012
DYNESYS
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NQP·March 28, 2012
DYNESYS UNKNOWN
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NQP·March 23, 2012
6.5MM REVERE PEDICLE SCREW 50MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code NQP·March 15, 2012
CD HORIZON AGILE SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC ORTHOPEDIC INC.·Product code NQP·March 19, 2009
CD HORIZON AGILE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code NQP·February 12, 2009
N-HANCE ROD
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code NQP·January 9, 2009
DYNESYS
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code NQP·March 18, 2009
CD HORIZON AGILE SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code NQP·February 5, 2009
CD HORIZON AGILE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code NQP·February 5, 2009