510(k) K243137 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal
Curiteva Porous PEEK Laminoplasty System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Oct 28, 2024 |
| Received | Sep 30, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243137
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.