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

Model Number	TPS-101-1112
Medical Device Problem Code	Appropriate Device Problem Term/Code Not Available (3191)
Health Effect - Clinical Code	Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Date of Event	10/05/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that during surgery a hole was discovered in the identity ps femur packaging for sn (b)(4).This breach was discovered after dr.Johnson had finished most of the femoral implant resections, barring the box resection.After discovering the packaging breach, they made a decision to bail on the procedure and move to zimmer.This caused a 30 minute+ delay.
Additional Manufacturer Narrative
It was reported that during surgery a hole was discovered in the identity ps femur packaging for sn (b)(4).This breach was discovered after dr.(b)(6) had finished most of the femoral implant resections, barring the box resection.After discovering the packaging breach, they made a decision to bail on the procedure and move to zimmer.This caused a 30 minute+ delay.The device history record was reviewed, and the implant was designed and manufactured per the specifications.All sterilisation requirements were met.

• Brand Name: ITOTAL IDENTITY PS
• Common Device Name: TOTAL KNEE REPLACEMENT SYSTEM
• Manufacturer (Section D): CONFORMIS, INC.; 600 technology park drive; billerica MA 01821
• Manufacturer (Section G): CONFORMIS, INC.; 600 research drive; wilmington MA 01887
• Manufacturer Contact: elizabeth haines ; 600 technology park drive; billerica, MA 01821
• MDR Report Key: 15739401
• Report Number: 3004153240-2022-00167
• Device Sequence Number: 16883698
• Product Code: JWH
• UDI-Device Identifier: M572TPS1011112011
• UDI-Public: M572TPS1011112011
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: K210252
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• 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): 11/04/2022

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: Health Professional
• Device Model Number: TPS-101-1112
• Device Catalogue Number: TPS-101-1112
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/05/2022
• Initial Report FDA Received Date: 11/04/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/18/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Age: 75 YR
• Patient Sex: Unknown