Model Number PPR6-7560 |
Device Problem
Insufficient Information (3190)
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Patient Problem
Osteolysis (2377)
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Event Type
Injury
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Manufacturer Narrative
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This complaint will be updated once the investigation is complete.Trends will be evaluated.
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Event Description
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Allegedly the patient was revised due to lysis socket; lysis stem.(b)(6).Side: r.Frasa: p1-fit and healthy.
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Manufacturer Narrative
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The deviced involved is not commercially available in the united states.Therefore the event is not reportable.Please void the initial report.
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Search Alerts/Recalls
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