510(k) K231809 · PML Bone Cement, Posterior Screw Augmentation
Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS Posterior Spinal Fixation System with G21 V-STEADY Bone Cement
| Applicant | Ulrich Medical USA, Plano TX, US |
| Decision | Substantially Equivalent, Oct 20, 2023 |
| Received | Jun 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231809
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.