It was reported as " event descriptions: tmk23137, kk, not enough external rotation in surgery.Tmk23228, mt, too much external rotation in surgery.Tmk23258, jg, left knee, following up on rotation issue.".
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Product complaint (b)(4).Investigation summary : the device associated with this report was not returned for evaluation.No evidence was found indicating product error was a contributing factor to the reported event.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional info be received, the investigation will be re-opened as necessary.
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