K242113
- 510(k) number
- K242113
- Device name
- Nerve Wrap (07-DW-001-TAB)
- Applicant
- Biocircuit Technologies, Inc. GA · US
- Product code
- JXI — Cuff, Nerve
- Decision date
- 2025-04-02
- Date received
- 2024-07-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242113.pdf
Official FDA record: K242113
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.