Catalog Number 150610005 |
Device Problem
Loss of or Failure to Bond (1068)
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Patient Problem
Not Applicable (3189)
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Event Date 07/24/2018 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Concomitant medical products: attune cr fem rt sz 6 nar cem, 150400226.Attune cr rp insrt sz 6 6mm, 151630606.
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Event Description
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Patient was revised to address aseptic loosening of the tibial components at the cement to implant interface.Cement manufacturer is competitor.The surgeon has expressed concern with the primary attune tibial tray in the past as he has revised multiples.Doi: (b)(6) 2015.Dor: (b)(6) 2018; right knee.
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Manufacturer Narrative
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Investigation summary: no device associated with this report was received for examination.If information is obtained that was not available for the initial medwatch , a follow-up medwatch, a follow-up medwatch will be filed as appropriate. .
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Search Alerts/Recalls
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