9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
A P HARNESS
FDA 510(k)
FDA Class 1
·General Hospital
NuVasive Cohere Thoracolumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
ZIMMER SEGMENTAL SYSTEM VARIABLE STIFFNESS STEM EXTENSIONS AND INTERCALARY SEGMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·February 27, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·August 5, 2014
MANUAL ORTHOPEDIC SURGICAL INSTRUMENT
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC·Product code HXB·February 8, 2011
BIOMET TIBIAL TRAYS
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·April 28, 2017
VANGUARD COMPLETE KNEE SYSTEM - PS OPEN INTL FEM-LT 67.5
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·April 28, 2017
VANGUARD PATELLA COMPONENTS -SERIES A PAT STD 31 3 PEG
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·April 28, 2017