FDA Device Intelligence
Home › Nuvasive, Inc. › NVM5

NVM5

Nuvasive, Inc. · Model 1581432 · UDI-DI 00887517090010

PDQHAWETNOLOIKNGWF Prescription
1
510(k) clearances
77
Adverse events (1 deaths)
2
Recalls
56
Facilities

Description

Brown/Black Paired 2.5m Needle Electrode

Recalls

DateFirmReason
2020-06-23The Magstim Company LimitedReports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator pod, may cause damage
2020-06-10NuVasive IncThe NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.