283 results
·
28ms
·
Sources: EU EUDAMED, US FDA
EBI, L.P.'S LINE EXTENSION TO THE ARRAY SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EBICE COLD THERAPY
FDA Adverse Event
Injury
·EBI, L.P.·Product code ILO·February 6, 2009
INTERGRO
FDA Adverse Event
Injury
·EBI, L.P.·Product code MQV·March 26, 2009
ARRAY SPINAL SYSTEM
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code MNI·January 21, 2009
VUELOCK IMPLANTS
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·March 6, 2009
T30 PROVISIONAL DRIVER
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code HXX·March 6, 2009
ARRAY TITATNIUM IMPLANTS, SCREW
FDA Adverse Event
Injury
·EBI, L.P.·Product code MNI·March 31, 2009
SPINAL LUMBAR IMPLANTS
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·March 16, 2009
C-TEK MAXAN IMPLANTS
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·March 6, 2009
SPINELINK
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·March 7, 2002
EBI XFIX DYNAFIX
FDA Adverse Event
Injury
·EBI, L.P.·Product code JEC·March 7, 2002
SPINELINK
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·March 7, 2002
EBI XFIX DYNAFIX
FDA Adverse Event
Injury
·EBI, L.P.·Product code HTY·November 6, 2003
OMEGA-21 SYSTEM
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code JDN·November 10, 2003
EBI
FDA Adverse Event
Other
·EBI, L.P.·Product code JDN·October 30, 2003
SPINELINK II
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KWQ·November 4, 2003
OMEGA-21 SYSTEM
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code JDN·October 22, 2003
EBI XFIX DYNAFIX
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KTT·November 6, 2003
SPINELINK II
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code JDN·October 22, 2003
EBI XFIX DYNAFIX
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code KTT·November 6, 2003