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At the time of this report, mentor has received no information regarding explantation or an expected explantation date.It is unknown at this time if the device will be made available for return.As a result, no product failure analysis can be conducted, and no determination of possible contributing factors can be made.As such, the investigation will be closed.If the complaint device is received in the future, the investigation will be reopened and conducted as appropriate.A manufacturing record evaluation (mre) was performed, and no anomalies were found related to this complaint.In addition, the mre verifies that the device was manufactured in accordance with documented specification and procedures.Mentor is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which mentor has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, mentor, or its employees that the report constitutes an admission that the device, mentor, or its employees caused or contributed to the potential event described in this report.Reason for device explant and/or reoperation: cutaneous contour deformity.Manufacturer¿s reference number: (b)(4).
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It was reported that a caucasian female patient enrolled in a clinical trial underwent a breast reconstruction surgery with 610cc mentor memoryshape breast implants.Post-operatively, the patient experienced wrinkling in both of her breasts, which required fat grafting and a pocket adjustment on (b)(6) 2020.At the time of this report, mentor has received no information regarding explantation or an expected explantation date.This report is for the left implant.Refer to manufacturing report number 1645337-2022-15410 for the contralateral event.
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