POLARIS ADJUSTABLE PRESSURE VALVE SHUNT POLARIS (R) VALVE SPV-400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2005-12-30 for POLARIS ADJUSTABLE PRESSURE VALVE SHUNT POLARIS (R) VALVE SPV-400 manufactured by Sophysa.

Event Text Entries

[36264218] The valve has been returned in (b)(4) 2005. Analysis has to be done. See sanned page.
Patient Sequence No: 1, Text Type: N, H10


[36264219] This polaris adjustable pressure valve was implanted to a pt in (b)(6). The implantation depth was less than 10 mm from the skin. In early (b)(6), the neurosurgeon attempted to decrease the setting pressure of the valve to 330 mmh2o ( or 230 mmh2o) with an adjustment magnet and a pressure selector, in vain. He replaced the valve with another spv-400 in (b)(6). He succeeded in changing the pressure of the explanted valve.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3001587388-2005-00384
MDR Report Key5345165
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2005-12-30
Date of Report2005-12-30
Date of Event2005-12-09
Date Mfgr Received2005-12-23
Date Added to Maude2016-01-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JEAN-CHRISTOPHE AUDRAS
Manufacturer Street22 RUE JEAN ROSTAND PARC CLUB ORSAY UNIVERSITE
Manufacturer CityORSAY, CEDEX F-91893
Manufacturer CountryFR
Manufacturer PostalF-91893
Manufacturer Phone69353500
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePOLARIS ADJUSTABLE PRESSURE VALVE SHUNT
Generic NameSHUNT, CENTRAL NERVOUS SYSTEM & COMPONENTS
Product CodeGYK
Date Received2005-12-30
Returned To Mfg2005-12-26
Model NumberPOLARIS (R) VALVE
Catalog NumberSPV-400
Lot NumberP0322
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSOPHYSA
Manufacturer Address22 RUE JEAN ROSTAND PARC CLUB ORSAY UNIVERSITE ORSAY, CEDEX F-91893 FR F-91893


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-12-30

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