510(k) K261632 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Thunderbolt System
| Applicant | Responsive Arthroscopy, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 20, 2026 |
| Received | May 18, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261632
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.