MAUDE Adverse Event Report: CONFORMIS, INC. ITOTAL G2; TOTAL KNEE REPLACEMENT SYSTEM

Model Number	TCR121111102
Health Effect - Clinical Code	Pain (1994)
Date of Event	06/01/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
It was reported that the patient had knee pains since receiving their implant.The patient went to a non-conformis surgeon where their implant was explanted and a full tka revision took place.The revising surgeon concluded that the conformis knee was "not working properly as it should".Review of the device history record indicates that the device was manufactured to specification.
Event or Problem Description
It was reported that the patient had knee pains since receiving their implant.The patient went to a non-conformis surgeon where their implant was explanted and a full tka revision took place.The revising surgeon concluded that the conformis knee was "not working properly as it should".

• Brand Name: ITOTAL G2
• Common Device Name: TOTAL KNEE REPLACEMENT SYSTEM
• Manufacturer (Section D): CONFORMIS, INC.; 600 technology park drive; billerica MA 01821
• MDR Report Key: 12021615
• Report Number: 3004153240-2021-00093
• Device Sequence Number: 14640480
• Product Code: JWH
• UDI-Device Identifier: M572TCR1211111021
• UDI-Public: +M572TCR1211111021
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K161366
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/17/2021

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: TCR121111102
• Device Catalogue Number: TCR-121-1111
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/01/2021
• Initial Report FDA Received Date: 06/17/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 59 YR