LHGClass IIImplant
Electrode, Spinal Epidural
Neurology · 21 CFR 882.5880
MDR events21All time
Recalls0All time
Registered firms4Currently listed
510(k) clearances1All time
Recent MDR events
21 adverse event reports on file
- LEAD DELIVERY SYS, 13 CM (5 IN), 1 EACHNov 2, 2015InjurySt. Jude Medical - Neuromodulation1627487-2015-07624
- LEAD DELIVERY SYS, 19CM (7.5 IN), 1 EACHSep 24, 2015InjurySt. Jude Medical - Neuromodulation1627487-2015-07562
- LEAD DELIVERY SYS, 19CM (7.5 IN), 1 EACHSep 24, 2015InjurySt. Jude Medical - Neuromodulation1627487-2015-07563
- LEAD DELIVERY SYS, 13 CM (5 IN), 1 EACHSep 24, 2015InjurySt. Jude Medical - Neuromodulation1627487-2015-07564
- RESUMEJun 16, 2004OtherNeuro2182207-2004-00792
- ITRELDec 11, 2003OtherNeuro2182207-2003-01157
- ITRELDec 13, 2001MalfunctionMedtronic Inc..6000030-2001-00967
- NAMar 10, 2000OtherMedtronic, Inc.2182207-2000-00090
- RESUME ILCMar 19, 1999MalfunctionMedtronic Inc.2182207-1999-00079
- SYMMIXAug 28, 1998MalfunctionMedtronic Inc.2182207-1997-00186
Event type breakdown
Malfunction9
Injury7
Other5
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
4 firms currently registered for this product code
510(k) clearances
1 clearances for this product code