MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. ADVANCE® II POST STAB TIBIAL INSERT SIZE 2 10MM; KNEE COMPONENT

Model Number	KIPS2210
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Type of Reportable Event	Serious Injury
Event or Problem Description
Allegedly, patient was revised due to peri-prosthetic fracture.No revised: part id kpontp35, advance onlay all poly patella 35mm tripeg, lot 29792865, qty 1.Revision njr number: (b)(4), side: r, primary asa: p2 - mild disease not incapacitating.
Additional Manufacturer Narrative
This event will be updated once the investigation is complete.Trends will be evaluated.
Additional Manufacturer Narrative
The additional information from reliability engineering is that he considered that this event should be changed to "no complaint stated" and there is no complaint against the device.Please void this report.

• Brand Name: ADVANCE® II POST STAB TIBIAL INSERT SIZE 2 10MM
• Common Device Name: KNEE COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer (Section G): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer Contact: 5677 airline road; arlington, TN 38002 ; 9018674771
• MDR Report Key: 13402007
• Report Number: 3010536692-2022-00031
• Device Sequence Number: 4858429
• Product Code: HRY
• UDI-Device Identifier: M684KIPS22101
• UDI-Public: M684KIPS22101
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K960617
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2009
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/08/2022

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: Other
• Device Model Number: KIPS2210
• Device Catalogue Number: KIPS2210
• Device Lot Number: 88692091
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 01/12/2022
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/12/2022
• Supplement Date Received by Manufacturer: 01/12/2022
• Initial Report FDA Received Date: 01/31/2022
• Supplement Report FDA Received Date: 02/08/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown