510(k) K173159 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Cervical Spinal Truss System (CSTS) Interbody Fusion Device
| Applicant | 4Web, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Jan 8, 2018 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173159
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.