ADVANTIM SMOOTH TIBIAL STEM 1870-0564

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 1999-11-22 for ADVANTIM SMOOTH TIBIAL STEM 1870-0564 manufactured by Wright Medical Technology, Inc..

Event Text Entries

[160868] Per letter from doctor, pt allegedly had "profound poly wear debris and subsequent osteolysis" on tibial spacer.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1043534-1999-00106
MDR Report Key251368
Report Source05
Date Received1999-11-22
Date of Report1999-10-21
Date of Event1998-10-30
Date Mfgr Received1999-10-21
Device Manufacturer Date1995-08-01
Date Added to Maude1999-11-30
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
Manufacturer ContactDEBBY DAURER
Manufacturer Street5677 AIRLINE RD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal38002
Manufacturer Phone9018674601
Manufacturer G1WRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Street5677 AIRLINE ROAD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal Code38002
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameADVANTIM SMOOTH TIBIAL STEM
Generic NameKNEE COMPONENT
Product CodeKRP
Date Received1999-11-22
Returned To Mfg1999-11-19
Model NumberNA
Catalog Number1870-0564
Lot Number085A024044
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeNO INFO
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key243512
ManufacturerWRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Address5677 AIRLINE RD. ARLINGTON TN 38002 US
Baseline Brand NameADVANTIM SMOOTH TIBIAL STEM
Baseline Generic NameKNEE COMPONENT
Baseline Catalog No1870-0564
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 1999-11-22

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