MOTO PARTIAL KNEE TIBIAL INSERT FIX S6 RM - 8MM 02.18.IF6.08.RM

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 2020-02-04 for MOTO PARTIAL KNEE TIBIAL INSERT FIX S6 RM - 8MM 02.18.IF6.08.RM manufactured by Medacta International Sa.

Event Text Entries

[177803184] Batch review performed on 09 january 2020: lot 167829: (b)(4) items manufactured and released on 14-dec-2016. Expiration date: 2021-11-29. No anomalies found related to the problem. To date, (b)(4) items of the same lot have been already sold without any other similar reported event.
Patient Sequence No: 1, Text Type: N, H10


[177803185] The patient came in reporting pain due to a hematoma in the knee. The cause of the hematoma is unknown. The surgeon performed an washout and poly-swap almost 3 weeks after primary. The surgery was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005180920-2020-00022
MDR Report Key9664310
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-02-04
Date of Report2020-02-04
Date of Event2020-01-07
Date Mfgr Received2020-01-07
Device Manufacturer Date2016-12-14
Date Added to Maude2020-02-04
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 STEFANO BAJ
Manufacturer StreetSTRADA REGINA
Manufacturer CityCASTEL SAN PIETRO, SWITZERLAND 6874
Manufacturer CountrySZ
Manufacturer Postal6874
Manufacturer G1MEDACTA INTERNATIONAL SA
Manufacturer StreetSTRADA REGINA
Manufacturer CityCASTEL SAN PIETRO, 6874
Manufacturer CountrySZ
Manufacturer Postal Code6874
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMOTO PARTIAL KNEE TIBIAL INSERT FIX S6 RM - 8MM
Generic NameKNEE TIBIAL INSERT
Product CodeHSX
Date Received2020-02-04
Model Number02.18.IF6.08.RM
Catalog Number02.18.IF6.08.RM
Lot Number167829
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDACTA INTERNATIONAL SA
Manufacturer AddressSTRADA REGINA CASTEL SAN PIETRO, 6874 SZ 6874


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-04

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