3D KNEE 392-11-710

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-25 for 3D KNEE 392-11-710 manufactured by Encore Medical L.p..

Event Text Entries

[186137999] Additional reporting on this event will be provided as a supplemental report to this document as soon as it becomes available.
Patient Sequence No: 1, Text Type: N, H10


[186138003] Revision surgery - lysis due to back side wear.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644408-2020-00256
MDR Report Key9878912
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-25
Date of Report2020-03-24
Date of Event2020-02-24
Date Mfgr Received2020-02-24
Date Added to Maude2020-03-25
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 ContactTEFFANY HUTTO
Manufacturer Street9800 METRIC BLVD
Manufacturer CityAUSTIN, TX 78758-5445,
Manufacturer CountryUS
Manufacturer G1ENCORE MEDICAL L.P.
Manufacturer Street9800 METRIC BLVD
Manufacturer CityAUSTIN, TX 78758-5445,
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3D KNEE
Generic NameINSERT, 3D EX SZ 10RT 11MM
Product CodeOIY
Date Received2020-03-25
Model Number392-11-710
Catalog Number392-11-710
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENCORE MEDICAL L.P.
Manufacturer Address9800 METRIC BLVD AUSTIN, TX 78758-5445, US


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2020-03-25

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