510(k) K211057 · OWI Bone Fixation Cerclage, Sublaminar
LigaPASS® Spinal System, CD Horizon Spinal System
| Applicant | Medtronic, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, May 27, 2021 |
| Received | Apr 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211057
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.