K252020
- 510(k) number
- K252020
- Device name
- TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly
- Applicant
- Hand Biomechanics Lab, Inc. CA · US
- Product code
- HRX — Arthroscope
- Decision date
- 2025-10-15
- Date received
- 2025-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252020.pdf
Official FDA record: K252020
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.