A review of the dhr demonstrated that the mid-c system was manufactured, tested, and released according to apifix specifications.On 17-feb-2024 apifix was notified that patient (b)(6), index procedure (b)(6) 2023, is planned to undergo revision {re-adjustment} surgery on (b)(6) 2024 due to {apifix} screw migration. on 22-feb-2024 apifix was notified that patient (b)(6) underwent revision surgery on that day, during which the surgeon replaced the apifix screw with two 8.0x50 poly screws and an extender.A new mid-c 125 was also reportedly used despite no report of implant failure.Risk assessment: reoperation events are a known risk that was assessed and recorded by the product risk assessment dms-777 rev r; screw misplacement/migration is addressed in the ifu as potential risks associated with the mid-c system and spinal surgery generally.Screw misplacement at the index surgery may lead to migration, curve progression, or pull-out over time.Since optimal screw placement, in the middle of the pedicle, is a complex task, especially in the upper part of the spine where the pedicles are very small, this problem is mainly related to the surgeon's skills and the patient's anatomy.In addition, screw migration may also result from an infection.The event may be associated with pain.Apifix is closing this complaint but will continue to monitor this 'failure mode'; complaint trending will continue to monitor per post marketing surveillance procedure.If any further relevant information is identified, the complaint file will be reopened and a supplemental medwatch will be filed.
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