TL, SHORT BOLT, WIRE FIXATION, UNIVERSAL 54-1151

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-07-17 for TL, SHORT BOLT, WIRE FIXATION, UNIVERSAL 54-1151 manufactured by Orthofix Srl.

MAUDE Entry Details

Report Number9680825-2019-00047
MDR Report Key8798313
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-07-17
Date of Report2019-07-17
Date of Event2019-05-23
Date Mfgr Received2019-06-21
Date Added to Maude2019-07-17
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 ContactMR. ROBERTO DONADELLO
Manufacturer StreetVIA DELLE NAZIONI, 9
Manufacturer CityBUSSOLENGO, VERONA, ITALY 37012
Manufacturer CountryIT
Manufacturer Postal37012
Manufacturer G1ORTHOFIX SRL
Manufacturer StreetVIA DELLE NAZIONI, 9
Manufacturer CityBUSSOLENGO, VERONA, 37012
Manufacturer CountryIT
Manufacturer Postal Code37012
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTL, SHORT BOLT, WIRE FIXATION, UNIVERSAL
Generic NameTL, SHORT BOLT, WIRE FIXATION, UNIVERSAL
Product CodeLXT
Date Received2019-07-17
Returned To Mfg2019-06-21
Model Number54-1151
Catalog Number54-1151
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerORTHOFIX SRL
Manufacturer AddressVIA DELLE NAZIONI, 9 BUSSOLENGO, VERONA, 37012 IT 37012


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-17

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