MAUDE Adverse Event Report: TREACE MEDICAL CONCEPTS 1ST MET INSERTER, GEN II; PLATE

Model Number	02-00198
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	11/06/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
It was reported that during an initial bunion surgery, the medial cortex was fractured.No other patient outcomes were reported as a result of this event.Additional information indicates the patient was a large male and had a prior bunionectomy.The medial side of the metatarsal was previously shaved, which may have weakened it.It was further reported the surgeon may have aggressively translated.No device was returned for evaluation as no deficiencies or malfunctions were alleged/found with any tmc device.No devices were returned for evaluation as the hardware remains implanted.Device-specific information was not available; therefore, a review of device history records was not able to be performed.However, all non-conformances for possible devices utilized in surgery were reviewed and no non-conformances or issues during the manufacture or release of the products were identified to date that could have contributed to what was reported.However, additional information indicates that the patient's size, prior bunionectomy, and the operator's technique may have contributed to what the patient experienced.The company will supplement this mdr as necessary and appropriate.
Event or Problem Description
It was reported that during an initial bunion surgery, the medial cortex was fractured.There were no deficiencies or malfunctions alleged/found with any tmc device and no other patient outcomes were reported as a result of this event.
Additional Manufacturer Narrative
H11.Corrected manufacturer narrative: it was reported that during an initial bunion surgery, the medial cortex was fractured.No other patient outcomes were reported as a result of this event.Additional information indicates the patient was a large male and had a prior bunionectomy.The medial side of the metatarsal was previously shaved, which may have weakened it.It was further reported the surgeon may have aggressively translated.No device was returned for evaluation as no deficiencies or malfunctions were alleged/found with any tmc device.Device-specific information was not available; therefore, a review of device history records was not able to be performed.However, all non-conformances for possible devices utilized in surgery were reviewed and no non-conformances or issues during the manufacture or release of the products were identified to date that could have contributed to what was reported.Although a number of factors could have contributed to what was reported, the most likely cause of the reported event could not be determined.However, additional information indicates that the patient's size, prior bunionectomy, and the operator's technique may have contributed to what the patient experienced.The company will supplement this mdr as necessary and appropriate.

• Brand Name: 1ST MET INSERTER, GEN II
• Common Device Name: PLATE
• Manufacturer (Section D): TREACE MEDICAL CONCEPTS; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer (Section G): TREACE MEDICAL CONCEPTS; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer Contact: renae ginter ; 100 palmetto park place; ponte vedra, FL ; 9043735940
• MDR Report Key: 20832915
• Report Number: 3011623994-2024-00226
• Device Sequence Number: 8627931
• Product Code: HRS
• UDI-Device Identifier: 00810111222884
• UDI-Public: (01)00810111222884
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K240173
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/03/2024

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: 02-00198
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/06/2024
• Supplement Date Received by Manufacturer: 11/06/2024
• Initial Report FDA Received Date: 12/03/2024
• Supplement Report FDA Received Date: 12/03/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): No
• 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: Other
• Patient Sex: Male