PYRAMESH C TITANIUM MESH G905H166

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 2019-10-26 for PYRAMESH C TITANIUM MESH G905H166 manufactured by Warsaw Orthopedics.

MAUDE Entry Details

Report Number1030489-2019-01216
MDR Report Key9243289
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-26
Date of Report2019-10-26
Date Mfgr Received2019-09-27
Device Manufacturer Date2016-12-20
Date Added to Maude2019-10-26
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 ContactSTACIE ZIEMBA
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal38132
Manufacturer Phone9013963133
Manufacturer G1WARSAW ORTHOPEDICS
Manufacturer Street2500 SILVEUS CROSSING
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePYRAMESH C TITANIUM MESH
Generic NameMESH, METAL
Product CodeEZX
Date Received2019-10-26
Model NumberNA
Catalog NumberG905H166
Lot Number0534630W
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerWARSAW ORTHOPEDICS
Manufacturer Address2500 SILVEUS CROSSING WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-10-26

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