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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION EON MINI; SCS IPG

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ST. JUDE MEDICAL - NEUROMODULATION EON MINI; SCS IPG Back to Search Results
Model Number 3788
Device Problem Pocket Stimulation (1463)
Patient Problems Undesired Nerve Stimulation (1980); Pain (1994); Inadequate Pain Relief (2388)
Event Date 05/07/2014
Event Type  Injury  
Event Description
Device 2 of 2.Reference mfr report: 1627487-2014-15407.
 
Manufacturer Narrative
Sjm has limited info related to the pt's med history and is unable to form an opinion as to the relevancy of the pt's history to the event reported.Sjm defers to the pt's physician regarding med history.
 
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Brand Name
EON MINI
Type of Device
SCS IPG
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
toi milner
6901 preston rd.
plano, TX 75024
9723098107
MDR Report Key3900113
MDR Text Key4647694
Report Number1627487-2014-15408
Device Sequence Number1
Product Code GZB
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
P010032
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 05/07/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date02/01/2016
Device Model Number3788
Device Lot Number4470792
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 05/07/2014
Initial Date FDA Received05/28/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured02/01/2014
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Treatment
SCS ANCHOR, MODEL 1192 (2),; IMPLANT DATE:
Patient Outcome(s) Other;
Patient Age42 YR
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