The associated complaint device was not returned.Without the actual product involved and/or device information, a manufacturing review cannot be performed and our investigation cannot proceed.The clinical/medical team concluded, no clinical relevant supporting documents were provided for inclusion in the clinical assessment.No medical assessment can be performed at this time.If the device or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.We consider this investigation closed.
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