6210S NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2004-02-25 for 6210S NA manufactured by Medtronic Inc., Cardiac Rhythm Management Division.

MAUDE Entry Details

Report Number2182208-2003-00395
MDR Report Key631199
Report Source05,06
Date Received2004-02-25
Date of Report2003-12-26
Date of Event2003-12-24
Date Mfgr Received2003-12-29
Device Manufacturer Date2003-03-05
Date Added to Maude2005-08-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNI
Event Type3
Type of Report3

Device Details

Generic NamePERMANENT LEAD INTRODUCER
Product CodeDTF
Date Received2004-02-25
Model Number6210S
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age11 MO
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedA
Device Sequence No1
Device Event Key620794
ManufacturerMEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION
Manufacturer AddressRICE CREEK CENTER 7000 CENTRAL AVE., NE / T279 MINNEAPOLIS MN *357 * SP
Baseline Brand NameNA
Baseline Generic NamePERMANENT LEAD INTRODUCER
Baseline Model No6210S
Baseline Catalog NoNA
Baseline IDNA
Baseline Device FamilyPERMANENT LEAD INTRODUCER
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]24
Baseline PMA FlagY
Premarket ApprovalK8427
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Life Threatening; 3. Required No Informationntervention 2004-02-25

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