PRSVN MB TIB TRAY LM/RL CEM S3 149826003

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 2005-02-11 for PRSVN MB TIB TRAY LM/RL CEM S3 149826003 manufactured by Depuy-cork, A Division Of Depuy Orthopaedics.

Event Text Entries

[393331] Pt was revised due to pain, discomfort, poor alignment and medial laxity.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2005-00142
MDR Report Key572311
Report Source05,08
Date Received2005-02-11
Date of Report2005-02-01
Date of Event2005-02-01
Date Facility Aware2005-02-01
Report Date2005-02-01
Date Mfgr Received2005-02-01
Device Manufacturer Date2003-04-01
Date Added to Maude2005-02-14
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
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 S3
Generic NameTOTAL KNEE REPLACEMENT
Product CodeMBD
Date Received2005-02-11
Returned To Mfg2005-02-07
Model NumberNA
Catalog Number149826003
Lot Number1087050
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age2 MO
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key562186
ManufacturerDEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS
Manufacturer AddressLOUGHBEY RINGASKIDDY COUNTY, CORK EI
Baseline Brand NamePRSVN MB TIB TRAY LM/RL CEM S3
Baseline Generic NameKNEE INSERT
Baseline Model NoNA
Baseline Catalog No149826003
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 2005-02-11

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