3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PULSE GEN MODEL 102
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 6, 2014
RESTORE SENSOR
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LGW·December 3, 2012
OCTRODE TRIAL LEAD
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 2, 2010