MODIFIED BECK ELEVATOR N/A SP-2359

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-09-10 for MODIFIED BECK ELEVATOR N/A SP-2359 manufactured by Biomet Microfixation.

MAUDE Entry Details

Report Number0001032347-2019-00412
MDR Report Key8986801
Report SourceUSER FACILITY
Date Received2019-09-10
Date of Report2019-11-30
Date of Event2019-08-14
Date Mfgr Received2019-11-26
Device Manufacturer Date2018-10-01
Date Added to Maude2019-09-10
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. CHRISTOPHER PAPPAS
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 NameMODIFIED BECK ELEVATOR
Generic NameELEVATOR, SURGICAL, DENTAL
Product CodeEMJ
Date Received2019-09-10
Model NumberN/A
Catalog NumberSP-2359
Lot Number100118I18
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.