PRSVN MB INSERT SZ3 11.5MM 149815310

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 2007-01-02 for PRSVN MB INSERT SZ3 11.5MM 149815310 manufactured by Depuy Orthopaedics, Depuy-cork.

Event Text Entries

[589163] Patient was revised to address pain in the knee.
Patient Sequence No: 1, Text Type: D, B5


[7914103] This complaint is still under investigation. Depuy will notify the fda of the results of this investigation once it has been completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1818910-2006-04336
MDR Report Key801160
Report Source05,08
Date Received2007-01-02
Date of Report2006-12-12
Date of Event2006-12-12
Date Mfgr Received2006-12-12
Date Added to Maude2007-01-09
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 Location0
Manufacturer ContactGINNY STAMBERGER, MGR
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone5743727333
Manufacturer G1DEPUY ORTHOPAEDICS
Manufacturer StreetLOUGHBEG
Manufacturer CityRINGASKIDDY CTY, CORK
Manufacturer CountryEI
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NamePRSVN MB INSERT SZ3 11.5MM
Generic Name87MBD
Product CodeMBD
Date Received2007-01-02
Model NumberNA
Catalog Number149815310
Lot Number1044192
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key788700
ManufacturerDEPUY ORTHOPAEDICS, DEPUY-CORK
Manufacturer AddressLOUGHBEG RINGASKIDDY CTY, CORK EI
Baseline Brand NamePRSVN MB INSERT SZ3 11.5MM
Baseline Generic NameKNEE INSERT
Baseline Model NoNA
Baseline Catalog No149815310
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 2007-01-02

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