510(k) K232150 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ZSFab Cervical Interbody System
| Applicant | Zsfab, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Aug 18, 2023 |
| Received | Jul 19, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232150
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.