510(k) K240838 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Spectrum Spine Cervical Cage System
| Applicant | Spectrum Spine, Inc., Jasper GA, US |
| Decision | Substantially Equivalent, May 30, 2024 |
| Received | Mar 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240838
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.