C-STEM PMMA END CAP 961226000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-11-22 for C-STEM PMMA END CAP 961226000 manufactured by Depuy International Ltd - 8010379.

MAUDE Entry Details

Report Number1818910-2019-117602
MDR Report Key9363241
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-22
Date of Report2019-10-28
Date of Event2019-11-21
Date Mfgr Received2019-11-22
Device Manufacturer Date2009-10-01
Date Added to Maude2019-11-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DR.
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY INT'L LTD. 8010379
Manufacturer StreetST ANTHONYS ROAD
Manufacturer CityLEEDS LS118 DT
Manufacturer CountryUK
Manufacturer Postal CodeLS11 8 DT
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameC-STEM PMMA END CAP
Generic NameHIP MISCELLANEOUS : CEMENT CENTRALIZER/PLUG
Product CodeJDK
Date Received2019-11-22
Catalog Number961226000
Lot Number2967886
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY INTERNATIONAL LTD - 8010379
Manufacturer AddressST. ANTHONY'S ROAD LEEDS LS118DT UK LS11 8DT


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-22

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