DeviceClearance

NUVASIVE NEURO VISION SYSTEM— 510(k) K090298

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K090298 for NUVASIVE NEURO VISION SYSTEM, Substantially Equivalent on 2009-06-08. Applicant: Nuvasive, Inc..

Clearance details

Applicant
Nuvasive, Inc.
Product code
Code GWF
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Diego, CA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code GWF

product code GWF
Malfunction
2,364
Other
4
Total
2,368

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.