510(k) K213359 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
SeaSpine WaveForm, C Interbody System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Dec 9, 2021 |
| Received | Oct 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213359
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.