2,797 results
·
30ms
·
Sources: EU EUDAMED, US FDA
AERO AL INSERTER - DISTRACTOR
FDA Adverse Event
Injury
·STRYKER SPINE-FRANCE·Product code LXH·March 24, 2015
OP-1
FDA Adverse Event
STRYKER BIOTECH·Product code MPY·February 22, 2008
UNK - CAGE/SPACERS: CONTACT FUSION
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 6, 2021
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·August 5, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·August 5, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 5, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 5, 2015
CALSTRUX
FDA Adverse Event
Product code MPY·February 22, 2008
MEDLINE INDUSTRIES, INC.
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, INC.·Product code FDE·September 16, 2024
UNK - CAGE/SPACERS: CONTACT FUSION
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 6, 2021
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 20, 2024
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 20, 2024
GEN LAPAROSCOPY #536335-P-LF
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES LP·Product code FDE·October 14, 2024
1030489-2017-00539
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code MQP·March 15, 2017
1030489-2017-00542
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code HWC·March 15, 2017
1030489-2017-00545
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code MAX·March 15, 2017
PROBE
FDA Adverse Event
MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXB·February 3, 2015
XIA II HOOK FORCEPS
FDA Adverse Event
Malfunction
·STRYKER SPINE BORDEUX·Product code LXH·January 2, 2009
XIA BLOCKER
FDA Adverse Event
Injury
·STRYKER SPINE BORDEAUX·Product code KWP·December 13, 2005
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWP·July 16, 2008