MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 3/10 MM R; KNEE INSERT PE

Model Number	02.12.E0310CRR
Health Effect - Clinical Code	Unspecified Tissue Injury (4559)
Date of Event	07/19/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
At 5 days after the primary, the patient came in reporting pain due to a quad tendon rupture and the cause is unknown.The surgeon performed a quad tendon repair and upsized the poly.The surgery was completed successfully.
Additional Manufacturer Narrative
Batch review performed on 29 july 2022.Lot 2112612: (b)(4) items manufactured and released on 01-dec-2021.Expiration date: 2026-11-17.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold without any similar reported event during the period of review.

• Brand Name: GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 3/10 MM R
• Common Device Name: KNEE INSERT PE
• Manufacturer (Section D): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, 6874 ; SZ 6874
• Manufacturer (Section G): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, 6874 ; SZ 6874
• Manufacturer Contact: stefano baj ; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• MDR Report Key: 15240605
• Report Number: 3005180920-2022-00613
• Device Sequence Number: 4693177
• Product Code: JWH
• UDI-Device Identifier: 07630971261501
• UDI-Public: 07630971261501
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: K202022
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• 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): 08/17/2022

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.E0310CRR
• Device Catalogue Number: 02.12.E0310CRR
• Device Lot Number: 2112612
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/19/2022
• Initial Report FDA Received Date: 08/17/2022
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/01/2021
• 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 Sex: Female