28 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018
PEDICLE SCREW 7X50
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018
PEDICLE SCREW 5X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018
M.U.S.T. RODS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026
PEDICLE SCREW PEDICLE SCREW 5X40
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024
M.U.S.T. POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024
MUST PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017
PEDICLE SCREW - PEDICLE SCREW 8X75MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·October 11, 2018
PEDICLE SCREW PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·September 9, 2022
MECTALIF OBLIQUE (TI PEEK) INTERBODY FUSION DEVICE 12X28X11 L10
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·April 1, 2020
M.U.S.T. PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017
PEDICLE SCREW 6X50
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·December 22, 2022
PEDICLE SCREW PEDICLE SCREW 6X40
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018
PEDICLE SCREW PEDICLE SCREW 7X45 (2 PCS)
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KWP·July 4, 2018
MUST ROD TI 5.5X480
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KWP·June 1, 2017
STRATA 2 VALVE, REGULAR
FDA Adverse Event
Injury
·MEDTRONIC NEUROSURGERY·Product code JXG·May 20, 2014
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 25, 2012
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code FZP·August 9, 2007
PEDICLE SCREW ROD COCR 5.5X200
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KWP·July 18, 2019
BENT ROD TI 5.5X75MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·January 27, 2022