K231117

Substantially Equivalent

neXus Ultrasonic Surgical Aspirator System

Applicant
Misonix, LLC, A Bioventus Company
Product code
LFL
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Farmingdale, NY, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code LFL

product code LFL
Death
29
Injury
1,046
Malfunction
21,642
Total
22,717

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.