K261448
- 510(k) number
- K261448
- Device name
- neXus Ultrasonic Surgical Aspirator System
- Applicant
- Misonix, LLC NY · US
- Product code
- LFL — Instrument, Ultrasonic Surgical
- Decision date
- 2026-07-30
- Date received
- 2026-05-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K261448.pdf
Official FDA record: K261448
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.