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 2005-05-24 for PRSVN MB TIB TRAY LM/RL CEM S2 149826002 manufactured by Depuy-cork, A Division Of Depuy Orthopaedics.

Event Text Entries

[370213] Bilateral patient was revised due to loosening of the tibial components.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2005-00763
MDR Report Key604769
Report Source05,08
Date Received2005-05-24
Date of Report2005-05-19
Date of Event2005-05-19
Date Facility Aware2005-05-19
Report Date2005-05-19
Date Mfgr Received2005-05-19
Device Manufacturer Date2002-06-01
Date Added to Maude2005-05-25
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 ContactGINNY STAMBERGER, MGR.
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone5743727333
Manufacturer G1DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS
Manufacturer StreetLOUGHBEY
Manufacturer CityRINGASKIDDY COUNTY, CORK
Manufacturer CountryEI
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 Received2005-05-24
Model NumberNA
Catalog Number149826002
Lot Number1096985
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age1 YR
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key594556
ManufacturerDEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS
Manufacturer AddressLOUGHBEY RINGASKIDDY COUNTY, CORK EI
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 2005-05-24

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