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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.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-05-06VAIVoluntary action indicatedNuVasive Specialized Orthopedics, Inc.12
2024-01-18NAINo action indicatedNuvasive PR, Inc.0
2019-12-09NAINo action indicatedNuvasive PR, Inc.0
2019-07-29NAINo action indicatedNuVasive, Inc0
2017-05-31NAINo action indicatedNuvasive PR, Inc.0
2017-05-26VAIVoluntary action indicatedNuVasive Inc2
2017-05-26VAIVoluntary action indicatedNuVasive Inc2
2017-05-04VAIVoluntary action indicatedNuVasive, Inc3
2016-10-26VAIVoluntary action indicatedNuvasive Inc2
2014-11-19NAINo action indicatedNuVasive Inc0
2014-11-19NAINo action indicatedNuVasive Inc0
2014-08-27NAINo action indicatedNuvasive Inc4
2014-04-01NAINo action indicatedNuvasive PR, Inc.0
2014-02-20NAINo action indicatedNuVasive Specialized Orthopedics, Inc.0
2014-02-05NAINo action indicatedNuVasive Inc0
2014-02-05NAINo action indicatedNuVasive Inc0
2013-03-12WLWarning LetterNuVasive Inc
2013-03-12WLWarning LetterNuVasive Inc
2012-11-02OAIOfficial action indicatedNuVasive Inc0
2012-11-02OAIOfficial action indicatedNuVasive Inc0
2012-02-10NAINo action indicatedNuVasive Inc0
2012-02-10NAINo action indicatedNuVasive Inc0
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