MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE NONPOROUS SZ 4+; KNEE COMPONENT

Model Number	KTCCNP41
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Code	No Information (3190)
Type of Reportable Event	Serious Injury
Event or Problem Description
Allegedly, patient was revised due to aseptic loosening femur; aseptic loosening tibia component not revised: patella.Revision njr number: (b)(6).Side: r.Primary asa: p1 - fit and healthy.

• Brand Name: ADVANCE® II COCR TIBIAL BASE NONPOROUS SZ 4+
• Common Device Name: KNEE COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• MDR Report Key: 10179236
• Report Number: 3010536692-2020-00391
• Device Sequence Number: 11403203
• Product Code: HRY
• UDI-Device Identifier: M684KTCCNP411
• UDI-Public: M684KTCCNP411
• Combination Product (Y/N): N
• Initial Reporter Country: GB
• PMA/510(K) Number: K960617
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2003
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/22/2020

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: KTCCNP41
• Device Catalogue Number: KTCCNP41
• Device Lot Number: 9355188
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 06/08/2020
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/08/2020
• Initial Report FDA Received Date: 06/22/2020
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention