510(k) K233414 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Shoreline ACS Interbody System; Shoreline RT Interbody System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 28, 2023 |
| Received | Oct 10, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233414
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.