K241700
- 510(k) number
- K241700
- Device name
- Tenex 2nd Generation System
- Applicant
- Trice Medical, Inc. PA · US
- Product code
- LFL — Instrument, Ultrasonic Surgical
- Decision date
- 2024-11-18
- Date received
- 2024-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K241700.pdf
Official FDA record: K241700
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.