PRSVN MB TIB TRAY LM/RL CEM S2 149826002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2004-03-03 for PRSVN MB TIB TRAY LM/RL CEM S2 149826002 manufactured by Depuy International, Ltd..

Event Text Entries

[335097] The pt was revised due to loosened tibial and femoral uni components.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2004-00137
MDR Report Key513928
Report Source05,08
Date Received2004-03-03
Date of Report2004-02-05
Date of Event2004-02-05
Date Facility Aware2004-02-05
Report Date2004-02-05
Date Mfgr Received2004-02-05
Date Added to Maude2004-03-04
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 ContactHANS KUSSEROW, MGR.
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone5743727416
Manufacturer G1DEPUY INTERNATIONAL, LTD.
Manufacturer StreetST. ANTHONY'S RD
Manufacturer CityBEESTON, LEEDS LS118DT
Manufacturer CountryUK
Manufacturer Postal CodeLS11 8DT
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NamePRSVN MB TIB TRAY LM/RL CEM S2
Generic NameTOTAL KNEE REPLACEMENT
Product CodeMBD
Date Received2004-03-03
Model NumberNA
Catalog Number149826002
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key502938
ManufacturerDEPUY INTERNATIONAL, LTD.
Manufacturer AddressST. ANTHONY'S RD BEESTON, LEEDS UK LS11 8DT
Baseline Brand NamePRSVN MB TIB TRAY LM/RL CEM S2
Baseline Generic NameKNEE INSERT
Baseline Model NoNA
Baseline Catalog No149826002
Baseline IDNA
Baseline Device FamilyPRSVN MB INSERT
Baseline Shelf Life ContainedN
Baseline Shelf Life [Months]NA
Baseline PMA FlagY
Premarket ApprovalP9100
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2004-03-03

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