MEDPOR IMPLANT 7516

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2008-03-20 for MEDPOR IMPLANT 7516 manufactured by Porex Surgical.

Event Text Entries

[836852] The doctor stated that the patient received a medpor nasal dorsum implant in 2006 in a septorhinoplasty procedure. The doctor reported that a portion of the implant was removed in 2007 because of rejection.
Patient Sequence No: 1, Text Type: D, B5


[7948684] Following a review of the device history record for lot 7516-a056h18, it was determined that all processes and test criteria are within the medpor implant finished product specification.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1057129-2008-00010
MDR Report Key1017131
Report Source05
Date Received2008-03-20
Date of Report2008-03-14
Date of Event2006-06-08
Date Mfgr Received2008-02-12
Device Manufacturer Date2005-09-11
Date Added to Maude2009-12-30
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 FDA0
Event Location0
Manufacturer ContactKENT IVERSEN
Manufacturer Street15 DART ROAD
Manufacturer CityNEWNAN GA 30265
Manufacturer CountryUS
Manufacturer Postal30265
Manufacturer Phone6784791610
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEDPOR IMPLANT
Generic NameFACIAL RECONSTRUCTION
Product CodeEPP
Date Received2008-03-20
Model NumberNA
Catalog Number7516
Lot NumberA056H18
ID NumberNA
Device Expiration Date2005-09-11
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPOREX SURGICAL
Manufacturer Address15 DART ROAD NEWNAN GA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2008-03-20

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