MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. EVOLUTIONMP TIB KEELED NONPOR SIZE 6 STANDARD RIG; KNEE COMPONENT

Model Number ETPKN6SR

Device Problem Loss of Osseointegration (2408)

Patient Problem Insufficient Information (4580)

Event Type  Injury  

Manufacturer Narrative

This event will be updated once the investigation is complete.Trends will be evaluated.

Event Description

Allegedly, patient underwent r tkr on (b)(6) 2018.Revised on (b)(6) 2021 due to loosening of the tibia.Revising surgeon was offered mpo's tibial revision option as the femur was not loose and could have stayed in place.Surgeon decided to revise all components with another manufacturer's full revision system.(b)(6).(b)(4).

• Brand Name: EVOLUTIONMP TIB KEELED NONPOR SIZE 6 STANDARD RIG
• Type of Device: 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: 12132690
• MDR Text Key: 260416001
• Report Number: 3010536692-2021-00368
• Device Sequence Number: 1
• Product Code: HRY
• UDI-Device Identifier: M684ETPKN6SR1
• UDI-Public: M684ETPKN6SR1
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K093552
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 09/10/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/07/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Other
• Device Model Number: ETPKN6SR
• Device Catalogue Number: ETPKN6SR
• Device Lot Number: 1769489
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 06/20/2021
• Date Manufacturer Received: 06/20/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 52 YR