ATTUNE PS RP INSRT SZ 6 10MM 1516-50-610 151650610

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2020-03-31 for ATTUNE PS RP INSRT SZ 6 10MM 1516-50-610 151650610 manufactured by Depuy Ireland - 9616671.

Event Text Entries

[186809475] (b)(4). Initial reporter occupation: lawyer. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[186809476] Records indicate the patient received a right attune total knee arthroplasty. No allegations provided of patient injury or product failure, nor report of revision. Doi: (b)(6) 2018; dor: unknown (right).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2020-09697
MDR Report Key9902545
Report SourceCONSUMER,OTHER
Date Received2020-03-31
Date of Report2020-03-12
Date of Event2019-08-05
Date Mfgr Received2020-03-12
Device Manufacturer Date2017-08-29
Date Added to Maude2020-03-31
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 ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DR.
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1CORK MFG & MATERIAL WAREHOUSE
Manufacturer StreetLOUGHBEG RINGASKIDDY
Manufacturer CityCORK
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATTUNE PS RP INSRT SZ 6 10MM
Generic NameATTUNE IMPLANT : KNEE TIBIAL INSERT
Product CodeNJL
Date Received2020-03-31
Model Number1516-50-610
Catalog Number151650610
Lot Number8595651
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY IRELAND - 9616671
Manufacturer AddressLOUGHBEG RINGASKIDDY CO. CORK EI


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-31

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