QUICK COUPLING FOR K-WIRES 511.791

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 2020-03-13 for QUICK COUPLING FOR K-WIRES 511.791 manufactured by Depuy Synthes Products Llc.

MAUDE Entry Details

Report Number8030965-2020-01851
MDR Report Key9831201
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-13
Date of Report2020-02-04
Date of Event2020-01-01
Date Mfgr Received2020-03-04
Device Manufacturer Date2013-04-16
Date Added to Maude2020-03-13
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 ContactKARA DITTY-BOVARD
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal4436
Manufacturer Phone6103142063
Manufacturer G1SYNTHES PRODUKTIONS GMBH
Manufacturer StreetHAUPTSTRASSE 24
Manufacturer CityWALDENBURG 4437
Manufacturer CountrySZ
Manufacturer Postal Code4437
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameQUICK COUPLING FOR K-WIRES
Generic NameDRIVER, SURGICAL, PIN
Product CodeGFC
Date Received2020-03-13
Returned To Mfg2020-02-12
Catalog Number511.791
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDEPUY SYNTHES PRODUCTS LLC
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-13

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