134 results
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55ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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SPIDER CERVICAL PLATING SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·February 4, 2011
SPIDER 2 LEVEL 39MM PLATE
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·March 8, 2012
SPIDER 3 LEVEL 59MM PLATE
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·March 8, 2012
IRIX-C CERVICAL INTEGRATED FUSION SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code OVE·November 23, 2016
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015
SPIDER CERVICAL PLATING SYSTEM SCREWS
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·March 7, 2012
FORTEX PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MNH·February 3, 2012
AXLE INTERSPINOUS FUSION SYSTEM SCREW DRIVER
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWP·March 8, 2012
CAPLESS LI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MNI·January 23, 2009
CAPLESS LI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MNI·January 23, 2009
CAPLESS LI PEDICLE 6.5-40MM SCREWS
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MNI·March 17, 2009
SPIDER CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·January 19, 2010
SPIDER CERVICAL PLATING (SCP) SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·October 29, 2014
SPIDER CERVICAL PLATING SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·May 18, 2012
SPIDER CERVICAL PLATING SYSTEM SCREWS
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code KWQ·March 7, 2012
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015
CALIX LUMBAR SPINAL IMPLANT SYSTEM
FDA Adverse Event
Injury
·X-SPINE SYSTEMS, INC.·Product code MAX·September 11, 2015