DISTAL FEMUR JTS UNK_STM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2020-03-11 for DISTAL FEMUR JTS UNK_STM manufactured by Stanmore Implants Worldwide.

MAUDE Entry Details

Report Number3004105610-2020-00054
MDR Report Key9817268
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2020-03-11
Date of Report2020-03-11
Date of Event2019-12-02
Date Mfgr Received2020-03-02
Device Manufacturer Date2017-12-08
Date Added to Maude2020-03-11
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 ContactMRS. DIANA ROGERS
Manufacturer Street210 CENTENNIAL AVENUE CENTENNIAL PARK, ELSTREE
Manufacturer CityBOREHAMWOOD WD6 3SJ
Manufacturer CountryGB
Manufacturer PostalWD6 3SJ
Manufacturer Phone2082386500
Manufacturer G1STANMORE IMPLANTS WORLDWIDE
Manufacturer Street210 CENTENNIAL AVENUE CENTENNIAL PARK, ELSTREE
Manufacturer CityBOREHAMWOOD WD6 3SJ
Manufacturer CountryGB
Manufacturer Postal CodeWD6 3SJ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDISTAL FEMUR JTS
Generic NamePROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER
Product CodeKRO
Date Received2020-03-11
Catalog NumberUNK_STM
Lot NumberPIN 21070
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTANMORE IMPLANTS WORLDWIDE
Manufacturer Address210 CENTENNIAL AVENUE CENTENNIAL PARK, ELSTREE BOREHAMWOOD WD6 3SJ GB WD6 3SJ


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-11

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