7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
AD-TECH EPIDURAL PEG ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
NuVasive Modulus XLIF Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
TARGET ADAPTER T2 SCN
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 21, 2012
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW, LLC·Product code MEB·January 8, 2013
BLUE RELOAD FOR ECHELON 60
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 2, 2010
SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·July 3, 2014