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Caliber Intramedullary Fixation System

FDA UDI
NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135963107·Caliber Kwire Guide The Caliber Intramedullary ...

IJS

FDA UDI
SKELETAL DYNAMICS L.L.C.·00841506105154·IJS-E K-Wire Guide, 1.5mm

UNSPECIFIED OZARK SCREW

FDA Adverse Event
Malfunction ·K2M, INC.·Product code KWG·June 9, 2022

UNSPECIFIED OZARK SCREW

FDA Adverse Event
Malfunction ·K2M, INC.·Product code KWG·June 9, 2022

LEFT THUMB CONDYLAR IMPLANT

FDA Adverse Event
Malfunction ·UNKNOWN·Product code KWG·April 22, 1996

CMC, TRAPEZIUM SIZE 20

FDA Adverse Event
Injury ·STRYKER GMBH·Product code KWG·November 17, 2017

TSRH 3D 6.5 X 50 MM SCREW, TI

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEKMANUFACTURING·Product code KWG·August 19, 2004

UNSPECIFIED OZARK SCREW

FDA Adverse Event
Malfunction ·K2M, INC.·Product code KWG·June 9, 2022

UNKNOWN ARPE CUP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019

UNKNOWN ARPE STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019

UNKNOWN ARPE NECK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

AE-QAS-SP42

FDA Adverse Event
Injury ·AESCULAP AG·Product code KWG·March 4, 2024

ARPE HEAD CURVE LONG +2

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWG·January 22, 2019

C8701, S ALEXIS LAP SYS W/KII FIOS 5/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code KWG·August 30, 2019

C8402, M ALEXIS O WND PROT/RET 5/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code KWG·December 13, 2019