Reportedly there was no patient involvement.Implant and explant dates: device is an instrument and is not implanted/explanted.Initial contact phone number: (b)(6).Pma 510(k): device is not distributed in the united states, but is similar to device marketed in the usa.Manufacturing location: (b)(4).Manufacturing date: september 24, 2008.No non-conformance reports were generated during production.Review of the device history record(s) showed that there were no issues during the manufacture of the product that would contribute to this complaint condition.A product investigation was completed: a visual inspection under 5x magnification, functional test, drawing review, and dimensional analysis were performed as part of this investigation.A definitive root cause cannot be identified with the limited complaint details.No new, unique or different patient harms were identified as a result of this evaluation.The design is adequate for its intended use when used and maintained as recommended, it did not contribute to the complaint condition.The device was returned with the tip of the coupling screw sheared off.Relevant dimensions could not be measured due to the returned condition however it is unlikely that the design contributed to the complaint condition.The design has since been obsolete and replaced with part 03.010.410.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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