PARTIAL ARTICULAR SURFACE LEFT MEDIAL SIZE F 11 MM THICKNESS N/A 42518200611

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-12-30 for PARTIAL ARTICULAR SURFACE LEFT MEDIAL SIZE F 11 MM THICKNESS N/A 42518200611 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

Report Number0001825034-2019-05607
MDR Report Key9532285
Report SourceHEALTH PROFESSIONAL
Date Received2019-12-30
Date of Report2020-03-19
Date of Event2019-11-22
Date Mfgr Received2020-03-17
Device Manufacturer Date2018-11-01
Date Added to Maude2019-12-30
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 ContactMS. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER BIOMET, INC.
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NamePARTIAL ARTICULAR SURFACE LEFT MEDIAL SIZE F 11 MM THICKNESS
Generic NamePROSTHESIS, KNEE
Product CodeHSX
Date Received2019-12-30
Returned To Mfg2020-01-30
Model NumberN/A
Catalog Number42518200611
Lot Number64157510
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-30

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