LATITUDE ELBOW PROSTHESIS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a literature report with the FDA on 2018-07-25 for LATITUDE ELBOW PROSTHESIS manufactured by Tornier Inc..

Event Text Entries

[115027755] This is the final report submitted regarding this surgical event and medical device.
Patient Sequence No: 1, Text Type: N, H10


[115027756] It was reported in the literature (pogliacomi, et al. 2015), the latitude prosthesis ((b)(4)) was implanted in 10 out of 20 surgeries. One patient required revision surgery 24 months after the first implant (latitude) as a consequence of aseptic loosening. No further patient complications have been reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004983210-2018-00035
MDR Report Key7719575
Report SourceLITERATURE
Date Received2018-07-25
Date of Report2018-07-25
Date Mfgr Received2018-06-25
Date Added to Maude2018-07-25
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 ContactMR. MATT KENNEDY
Manufacturer Street10801 NESBITT AVE S
Manufacturer CityBLOOMINGTON MN 55437
Manufacturer CountryUS
Manufacturer Postal55437
Manufacturer Phone9526837482
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLATITUDE ELBOW PROSTHESIS
Generic NameELBOW PROSTHESIS
Product CodeJDB
Date Received2018-07-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTORNIER INC.
Manufacturer Address10801 NESBITT AVENUE S BLOOMINGTON MN 55437 US 55437


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-07-25

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