The reported unknown zimmer titanium abutment was not returned.Since product hasn't been returned, visual/functional inspection could not be performed.The investigation has been performed based on the available information.No relevant pre-existing conditions were noted on the per.The reported device was located on an unknown tooth, and for an unknown period of time.Based on the evaluation and available information, the device malfunction could not be verified.No device lot number was provided so a device history record review and a complaint history review could not be performed.A singular root cause could not be determined.The following sections have been updated: b4: date of this report.D3: manufacturer.G1-g2: contact office - name/address.G4: date received by manufacturer.G7: type of report.H2: follow up type.H6: evaluation codes.H10: additional narrative/date.
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