510(k) K231232 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal
Curiteva Laminoplasty System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Jun 28, 2023 |
| Received | Apr 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231232
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.