MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA GMK-REVISION 02.07.0310PSF TIBIAL INSERT PS FIXED SIZE 3/10MM; KNEE TIBIAL INSERT PS FIXED

Catalog Number	02.07.0310PSF
Medical Device Problem Code	Device Appears to Trigger Rejection (1524)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	12/15/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
The patient had a primary knee surgery with competitor devices on unknown date.Subsequently, the patient was revised for an unknown reason on the (b)(6) 2023 and medacta devices were implanted.Presently, on (b)(6) 2023, the patient came in due to signs of infection and the pathogen is unknown.The surgeon performed a washout and revised the insert.The surgery was completed successfully.
Additional Manufacturer Narrative
Batch review performed on 22-dec-2023.Lot 1903558: (b)(4) items manufactured and released on 09-jul-2019.Expiration date: 2024-06-26.No anomalies found related to the problem.To date, 88 items of the same lot have been sold with no similar reported case during the period of review.

• Brand Name: GMK-REVISION 02.07.0310PSF TIBIAL INSERT PS FIXED SIZE 3/10MM
• Common Device Name: KNEE TIBIAL INSERT PS FIXED
• Manufacturer (Section D): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• Manufacturer (Section G): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• Manufacturer Contact: marco giannessi ; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• MDR Report Key: 18501915
• Report Number: 3005180920-2023-01079
• Device Sequence Number: 20799505
• Product Code: JWH
• UDI-Device Identifier: 07630030817069
• UDI-Public: 07630030817069
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• PMA/510(K) Number: K090988
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 01/12/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 06/26/2024
• Device Catalogue Number: 02.07.0310PSF
• Device Lot Number: 1903558
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/15/2023
• Initial Report FDA Received Date: 01/12/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/09/2019
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Male