HIFIX SKULL PIN AC020

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2005-12-27 for HIFIX SKULL PIN AC020 manufactured by Depuy Spine, Inc..

Event Text Entries

[430908] During application of a halo crown and jacket on a pt, it was noticed that one of the hifix halo pins had managed to penetrate through the patient's skull without the torque cap breaking as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1526439-2005-00279
MDR Report Key656867
Report Source01,07
Date Received2005-12-27
Date Facility Aware2005-12-27
Report Date2005-12-27
Date Mfgr Received2005-11-29
Date Added to Maude2005-12-29
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 ContactMATTHEW KING
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone5088283106
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameHIFIX SKULL PIN
Generic NameCOMPONENT, TRACTION, INVASIVE
Product CodeHAX
Date Received2005-12-27
Model NumberNA
Catalog NumberAC020
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key646352
ManufacturerDEPUY SPINE, INC.
Manufacturer Address325 PARAMOUNT DR. RAYNHAM MA 02767 US
Baseline Brand NameBREMER HALO SYSTEM
Baseline Generic NameHIFIX SKULL PIN
Baseline Model NoNA
Baseline Catalog NoAC020
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-12-27

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