K261632
- 510(k) number
- K261632
- Device name
- Thunderbolt System
- Applicant
- Responsive Arthroscopy, Inc. MN · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2026-07-20
- Date received
- 2026-05-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K261632.pdf
Official FDA record: K261632
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.