Date of event is estimated.Based on the information provided a device problem was not identified, as a result a conclusive cause for the reported patient effect, and the relationship to the product, if any, cannot be determined.
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Related manufacturer reference numbers: 1627487-2021-16989, 3006705815-2021-04565, 3006705815-2021-04564, 3006705815-2021-04563.It was reported that the patient is experiencing pain and discomfort at the implant site.As a result, the system was explanted to address the issue.
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