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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.

6 linked reportsMalfunction 6
12232022-03: 0 reports for this device; peer average 1/device2023-07: 0 reports for this device; peer average 1/device2025-01: 2 reports for this device; peer average 2/device2025-03: 1 reports for this device; peer average 1/device2025-04: 3 reports for this device; peer average 3/device2025-12: 0 reports for this device; peer average 1.5/device2026-03: 0 reports for this device; peer average 2/device03070103041203
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2022-0301
2023-0701
2025-0122
2025-0311
2025-0433
2025-1201.5
2026-0302
This device (reports/month)Average device in PGM (reports/device/month)
Failure-mode summaryAI-generated

6 linked report narratives available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-04-221030489-2025-01790MalfunctionAvailableexact di
2025-04-221030489-2025-01789MalfunctionAvailableexact di
2025-04-221030489-2025-01791MalfunctionAvailableexact di
2025-03-281030489-2025-01579MalfunctionAvailableexact di
2025-01-051030489-2025-00114MalfunctionAvailableexact di
2025-01-031030489-2025-00069MalfunctionAvailableexact di
Regulatory clearances

    Predicate lineage

    Cited as predicate by: K181068, K221646

    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
    2026-02-06NAINo action indicatedMedtronic Sofamor Danek USA Inc0
    2017-10-26NAINo action indicatedMedtronic Sofamor Danek USA, Inc0
    2015-11-03VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc0
    2015-10-23VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc1
    2014-03-11VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc0
    2013-07-15NAINo action indicatedMedtronic Sofamor Danek USA, Inc0
    2013-07-15NAINo action indicatedMedtronic Sofamor Danek USA Inc0
    2012-06-06VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc0
    2011-02-23NAINo action indicatedMedtronic Sofamor Danek Usa Inc0
    2010-08-06VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc0
    2010-03-04VAIVoluntary action indicatedMedtronic Sofamor Danek USA Inc0
    2010-02-25NAINo action indicatedMedtronic Sofamor Danek USA Inc0
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