MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA GMK TOTAL KNEE SYSTEM; GMK-SPHERIKA 02.12.KA13R FEMORAL COMPONENT SPHERIKA CEMENTED S3+R

Model Number	02.12.KA13R
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Loss of Range of Motion (2032)
Date of Event	03/25/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Batch review performed on 1 april 2025.Lot 2113673.(b)(4) items manufactured and released on 27/10/2021.Expiration date: 14/10/2026.No anomalies found related to the problem.To date, all items of the same lot have been sold with no similar reported event during the period of review.Other devices involved: gmk-spherika 02.07.1203r tibial tray fixed cemented size 3 r (k090988) lot 2337001: (b)(4) items manufactured and released on 16/11/2023.Expiration date: 20/10/2028.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold with no similar reported event during the period of review.Gmk-spherika 02.07.1203r tibial tray fixed cemented size 3 r (k090988) lot 2236014: (b)(4) items manufactured and released on 10/10/2022.Expiration date: 20/09/2027.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold with no similar reported event during the period of review.Based on the information available no definitive root cause can be established, while there is no indication that any potential issue with the device may have caused or contributed to the event, and the device history record review does not indicate any potential manufacturing related issue.
Event or Problem Description
The patient reported stiffness.About 1 year and 1 month after the primary surgery, the stiffness was treated under anesthesia with manipulation, but no component was revised.

• Brand Name: GMK TOTAL KNEE SYSTEM
• Common Device Name: GMK-SPHERIKA 02.12.KA13R FEMORAL COMPONENT SPHERIKA CEMENTED S3+R
• 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: 21897617
• Report Number: 3005180920-2025-00319
• Device Sequence Number: 19693631
• Product Code: JWH
• UDI-Device Identifier: 07630345716224
• UDI-Public: 07630345716224
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K211004
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 04/24/2025

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 Model Number: 02.12.KA13R
• Device Lot Number: 2113673
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/25/2025
• Initial Report FDA Received Date: 04/24/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/27/2021
• 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 Age: 56 YR
• Patient Sex: Female