DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD 1890-6312

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2000-06-20 for DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD 1890-6312 manufactured by Wright Medical Technology, Inc..

MAUDE Entry Details

Report Number1043534-1999-00089
MDR Report Key285085
Report Source06,07
Date Received2000-06-20
Date of Event1999-08-30
Date Mfgr Received1999-08-31
Device Manufacturer Date1998-04-01
Date Added to Maude2000-07-12
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 Location0
Manufacturer ContactDEBBY DAURER
Manufacturer Street5677 AIRLINE RD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal38002
Manufacturer Phone9018674601
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameDURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD
Generic NameKNEE COMPONENT
Product CodeKRP
Date Received2000-06-20
Model NumberNA
Catalog Number1890-6312
Lot Number048A079500
ID NumberNA
Device Availability*
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key275886
ManufacturerWRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Address5677 AIRLINE RD ARLINGTON TN 38002 US
Baseline Brand NameDURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD
Baseline Generic NameKNEE COMPONENT
Baseline Catalog No1890-6312
Baseline Device FamilyK J 888.3560
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2000-06-20

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