225 results · 41ms · Sources: EU EUDAMED, US FDA

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6000030-2005-00383

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·February 28, 2012

6000030-1997-00238

FDA Adverse Event
Malfunction ·MEDTRONIC INC·Product code LKK·August 29, 1997

6000030-2006-00073

FDA Adverse Event
Malfunction ·RICE CREEK MFG·Product code LKK·January 13, 2006

6000030-2007-00156

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·November 21, 2012

6000030-2015-00147

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code DTE·October 7, 2015

6000030-2010-06059

FDA Adverse Event
Injury ·RICE CREEK MANUFACTURING·August 12, 2010

INDURA

FDA Adverse Event
Injury ·RICE CREEK MANUFACTURING·Product code LKK·February 8, 2008

PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·January 19, 2018

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 10, 2012

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code LKK·September 30, 2013

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code LKK·February 14, 2013

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·May 17, 2016

SYNCHROMED EL

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 3, 2007

N'VISION

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 4, 2008

MEDTRONIC

FDA Adverse Event
Injury ·MEDTRONIC INC. USA·Product code LKK·February 15, 2005

ITREL 3

FDA Adverse Event
Death ·MED REL, INC.·Product code GZB·October 13, 2006

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·September 2, 2010

MEDTRONIC

FDA Adverse Event
Injury ·MEDTRONIC INC YSA·Product code LKK·December 30, 2004

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code LKK·March 19, 2010

MEDTRONIC

FDA Adverse Event
Malfunction ·MEDTRONIC INC. USA·Product code LKK·October 25, 2004