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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
  • 510(k)K140607Substantially equivalent (SESE) · 2014-05-08clearance family

Predicate lineage

Cited as predicate by: K161696, K230141

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
2025-09-11NAINo action indicatedAAP Implantate Ag0
2025-09-11NAINo action indicatedAAP Implantate Ag0
2022-11-04NAINo action indicatedAAP Implantate Ag0
2022-11-04NAINo action indicatedAAP Implantate Ag0
2019-11-07VAIVoluntary action indicatedAAP Implantate Ag6
2019-11-07VAIVoluntary action indicatedAAP Implantate Ag6
2017-05-17NAINo action indicatedAAP Implantate Ag0
2017-05-17NAINo action indicatedAAP Implantate Ag0
2015-02-12NAINo action indicatedAAP Implantate Ag0
2015-02-12NAINo action indicatedAAP Implantate Ag0
2012-03-15VAIVoluntary action indicatedAAP Implantate Ag4
2012-03-15VAIVoluntary action indicatedAAP Implantate Ag4
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