TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT N/A 24-6550

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-30 for TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT N/A 24-6550 manufactured by Biomet Microfixation.

MAUDE Entry Details

Report Number0001032347-2020-00182
MDR Report Key9897171
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-01-16
Date Mfgr Received2020-03-10
Device Manufacturer Date2015-01-01
Date Added to Maude2020-03-30
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. TORI SAWYER
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal32218
Manufacturer Phone9047414400
Manufacturer G1BIOMET MICROFIXATION
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal Code32218
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameTMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT
Generic NameJOINT, TEMPOROMANDIBULAR, IMPLANT
Product CodeLZD
Date Received2020-03-30
Model NumberN/A
Catalog Number24-6550
Lot Number575530B
Device Expiration Date2020-01-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-30

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