10 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth Electrodes, Spencer Probe Depth Electrodes
FDA 510(k)
FDA Class 2
·Neurology
DEPTH ELECTRODE
FDA Adverse Event
Malfunction
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021
SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS
FDA Adverse Event
Injury
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180529676·Extended Arsenal Tap 5.5mm
TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/14 MM L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·January 26, 2018
GDC 360 DETEACHABLE COIL
FDA 510(k)
FDA Class 2
·Neurology
D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EXCELLENCE+
FDA Adverse Event
Injury
·MPRI·Product code NVN·October 10, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL. LTD.·Product code KWA·July 8, 2011