510(k) K222256 · PML Bone Cement, Posterior Screw Augmentation
BonOs® Inject Bone Cement; NEO Pedicle Screw System
| Applicant | Neo Medical SA, Villette (Lavaux), CH |
| Decision | Substantially Equivalent, Aug 26, 2022 |
| Received | Jul 27, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K222256
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.