510(k) K261621 ยท QUW Mesh, Surgical, Non-Resorbable, Orthopedics, Reinforcement Of Ligament
TekBrace Solo Soft Tissue Reinforcement Device
| Applicant | Theramicro, Cordova TN, US |
| Decision | Substantially Equivalent, Jun 9, 2026 |
| Received | May 15, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261621
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.