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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

    Predicate lineage

    Cited as predicate by: K152237

    Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

    Manufacturer compliance record
    DateTypeOutcomeFacilityCitations
    2017-08-25NAINo action indicatedXTANT Medical Holdings, Inc0
    2017-08-25NAINo action indicatedXTANT Medical Holdings, Inc0
    2013-07-12VAIVoluntary action indicatedXTANT Medical Holdings, Inc1
    2013-07-12VAIVoluntary action indicatedXTANT Medical Holdings, Inc1
    2013-07-11NAINo action indicatedXTANT Medical Holdings, Inc0
    2013-07-11NAINo action indicatedXTANT Medical Holdings, Inc0
    2013-01-28WLWarning LetterXTANT Medical Holdings, Inc—
    2013-01-28WLWarning LetterXTANT Medical Holdings, Inc—
    2013-01-28WLWarning LetterXTANT Medical Holdings, Inc—
    2013-01-28WLWarning LetterXTANT Medical Holdings, Inc—
    2012-07-27OAIOfficial action indicatedXTANT Medical Holdings, Inc6
    2012-07-27OAIOfficial action indicatedXTANT Medical Holdings, Inc6
    2012-07-26OAIOfficial action indicatedXTANT Medical Holdings, Inc12
    2012-07-26OAIOfficial action indicatedXTANT Medical Holdings, Inc12
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