Zimmer biomet complaint number (b)(4).Patient identifier unknown / not provided.Age and date of birth unknown / not provided.Weight unknown / not provided.Date of the event unknown / not provided.Brand name unknown / not provided.Device product code unknown / not provided.Additional device information unknown / not provided.Email address was not provided.Premarket identification pma/510(k) number unknown / not provided.Device manufacturer date unknown / not provided.Since the lot number and device will not be returned , identifying a definitive root cause will not be possible.Should additional information be received which indicated that the device may have caused or contributed to the event, an additional report would be submitted.
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