510(k) K260286 · PML Bone Cement, Posterior Screw Augmentation
Dynamo Spinal Cement; Salvo® Spine System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jun 15, 2026 |
| Received | Jan 29, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260286
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.