The patient was revised to address pain and loosening of the tibial component at cement to implant interface.Unknown cement was used.The attune tibial baseplate and insert were removed on (b)(6) 2019 and an attune revision tibial baseplate, stem, augments, and insert were implanted.Doi: (b)(6) 2014.Dor: (b)(6) 2019, left knee.
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Depuy synthes is submitting this report pursuant to the provision of 21 cfr, part 803.The report may be based on the information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.Device history lot : null.Device history batch : null.Device history review : null.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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