ITST INTERTROCHANTERIC/SUBTROCHANTERIC FIXATION LAG SCREW 00225700137

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,07 report with the FDA on 2002-08-30 for ITST INTERTROCHANTERIC/SUBTROCHANTERIC FIXATION LAG SCREW 00225700137 manufactured by Zimmer, Inc..

Event Text Entries

[260631] Construct moved into varus. Anti-rotation and lag screw cut out of femoral head/neck. Devices removed and revised to a total hip.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1822565-2002-00104
MDR Report Key413918
Report Source01,05,07
Date Received2002-08-30
Date of Report2002-07-31
Date of Event2002-06-27
Date Facility Aware2002-07-31
Report Date2002-07-31
Date Mfgr Received2002-07-31
Date Added to Maude2002-09-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactCONNIE MORGAN, MANAGER
Manufacturer StreetP.O. BOX 708
Manufacturer CityWARSAW IN 465810708
Manufacturer CountryUS
Manufacturer Postal465810708
Manufacturer Phone5743724269
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameITST INTERTROCHANTERIC/SUBTROCHANTERIC FIXATION LAG SCREW
Generic NameLAG SCREW
Product CodeNDE
Date Received2002-08-30
Model NumberNA
Catalog Number00225700137
Lot NumberUNK
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Age20 DAY
Device Eval'ed by MfgrN
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key402957
ManufacturerZIMMER, INC.
Manufacturer AddressP.O. BOX 708 WARSAW IN 465810708 US
Baseline Brand NameITST INTERTROCHANTERIC/SUBTROCHANTERIC FIXATION LAG SCREW
Baseline Generic NameLAG SCREW
Baseline Model NoNA
Baseline Catalog No00225700137
Baseline IDNA
Baseline Device FamilyITST FIXATION
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2002-08-30

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