3D KNEE 392-09-712

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 2020-03-20 for 3D KNEE 392-09-712 manufactured by Encore Medical L.p..

Event Text Entries

[184422101] Additional reporting on this event will be provided as a supplemental report to these documents as soon as it becomes available.
Patient Sequence No: 1, Text Type: N, H10


[184422102] Revision surgery - due to instability.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644408-2020-00252
MDR Report Key9860738
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-20
Date of Report2020-03-17
Date of Event2020-02-20
Date Mfgr Received2020-02-20
Date Added to Maude2020-03-20
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 12RT 9MM
Product CodeOIY
Date Received2020-03-20
Model Number392-09-712
Catalog Number392-09-712
Lot Number332G1031
Device Expiration Date2019-11-30
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. Required No Informationntervention 2020-03-20

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