No device associated with this report was received for examination.A worldwide complaint database search made over the previous 10 years found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Corrective action was not indicated.Product complaint # (b)(4).Investigation summary no device associated with this report was received for examination.A worldwide complaint database search made over the previous 10 years found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Corrective action was not indicated.Device history lot null device history batch null device history review null depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on 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.H10 additional narrative: if information is obtained that was not available for the initial medwatch , a follow-up medwatch, a follow-up medwatch will be filed as appropriate. .
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