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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

    K080699

    Cited as predicate by: K100743, K110843, K112014, K133721, K141665, K143740, K160646, K162986, K180480, K180724

    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
    2017-04-19VAIVoluntary action indicatedAlphatec Spine, Inc.1
    2016-03-16VAIVoluntary action indicatedAlphatec Spine, Inc.1
    2015-07-16WLWarning LetterAlphatec Spine, Inc.—
    2015-03-13OAIOfficial action indicatedAlphatec Spine, Inc.0
    2013-06-14NAINo action indicatedAlphatec Spine, Inc.0
    2012-04-27VAIVoluntary action indicatedAlphatec Spine, Inc.0
    2011-01-11WLWarning LetterAlphatec Spine, Inc.—
    2010-12-13VAIVoluntary action indicatedAlphatec Spine, Inc.7
    2010-06-21WLWarning LetterAlphatec Spine, Inc.—
    2010-02-11OAIOfficial action indicatedAlphatec Spine, Inc.11
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