Catalog Number 0020600 |
Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problem
Failure of Implant (1924)
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Event Date 09/22/2017 |
Event Type
Injury
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Manufacturer Narrative
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This is the final report submitted regarding this surgical event and medical device.
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Event Description
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It was reported that a patient underwent a revision surgery due to loss of fixation.The implant classification is fracture.No other effects have been reported.
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Manufacturer Narrative
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This is the final report submitted regarding this surgical event and medical device.
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Event Description
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Original submission was submitted in error.It was discovered during investigation that the device was not a tornier device.
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Search Alerts/Recalls
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