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 08 report with the FDA on 2004-11-17 for PRSVN MB TIB TRAY LM/RL CEM S3 149826003 manufactured by Depuy International, Ltd..

Event Text Entries

[311252] Pt was revised due to loosening of tibial component.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2004-00804
MDR Report Key555229
Report Source08
Date Received2004-11-17
Date of Report2004-10-26
Date Facility Aware2004-10-26
Report Date2004-10-26
Date Mfgr Received2004-10-26
Device Manufacturer Date2002-12-01
Date Added to Maude2004-11-18
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 INTERNATIONAL, LTD.
Manufacturer StreetST. ANTHONY'S ROAD
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 S3
Generic NameTOTAL KNEE REPLACEMENT
Product CodeMBD
Date Received2004-11-17
Model NumberNA
Catalog Number149826003
Lot NumberYML69
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age1 YR
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key544877
ManufacturerDEPUY INTERNATIONAL, LTD.
Manufacturer AddressST. ANTHONY'S ROAD BEESTON, LEEDS UK LS11 8DT
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 2004-11-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.