The complaint sample was not returned to viant for evaluation.Thus, the reported event is non-verifiable.The ifu sent with this device today, man-004006 rev a, states the following; end of life is determined by wear and damage due to intended use.Visually inspect for damage and wear.If the instrument is damaged and worn it is considered at the end of its life and should be discarded.Where instruments form part of a larger assembly, check assembly with mating components.Each component of the viant offset reamer handle is not a medical device, all components when assembled create the medical device.Therefore, the components of each viant reamer handle form a unique set when assembled.In no instance should the components from one offset reamer handle be mixed with components from another reamer handle.The unique device identification for this medical device is located on the assembled offset reamer handle.Viant devices should only be used by qualified personnel fully trained in the use of the surgical instruments and the relevant surgical procedures.Do not modify viant instruments in any way and handle with care at all times.Surface scratches can increase wear and the risk of corrosion.Manual surgical instruments have a limited life-span which is determined by wear or damage due to repeated intended use.When a surgical instrument reaches the end of its functional life, clean the instrument of any and all biomaterial/biohazards and safely discard the instrument in accordance with applicable laws and regulations.The device history records (dhr) were reviewed and found no related manufacturing deviations or anomalies that would have contributed to the reported event.This device has experienced approximately 1.44 years of use.It is unknown how many surgical procedures (cycles) this device has experienced throughout its life in the field.In conclusion, the complaint sample was not received by viant for evaluation and the reported event is non-verifiable.If the complaint sample is received by viant, it will be evaluated, the complaint record will be updated accordingly, and a supplemental medwatch 3500a emdr will be submitted as well.No further investigation is required at this time.G2: complaint information provided by distributor, depuy synthes.
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