MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. ADVANCE PRIMARY FEMORAL SIZE 6 RIGHT NONPOROUS; KNEE COMPONENT

Model Number	KFTCNP6R
Health Effect - Clinical Code	Unspecified Infection (1930)
Type of Reportable Event	Serious Injury
Event or Problem Description
Allegedly, patient was revised due to infection.Revision njr number: (b)(4), side: r, primary asa: p2, mild disease not incapacitating.(b)(4).

• Brand Name: ADVANCE PRIMARY FEMORAL SIZE 6 RIGHT NONPOROUS
• Common Device Name: KNEE COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• MDR Report Key: 11403767
• Report Number: 3010536692-2021-00133
• Device Sequence Number: 4568215
• Product Code: MBH
• UDI-Device Identifier: M684KFTCNP6R1
• UDI-Public: M684KFTCNP6R1
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K972626
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2010
• Device Explanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 03/03/2021

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: KFTCNP6R
• Device Catalogue Number: KFTCNP6R
• Device Lot Number: 055213653
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 02/22/2021
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/22/2021
• Initial Report FDA Received Date: 03/03/2021
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention