510(k) K173175 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Paramount Anterior Cervical Cage System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Nov 1, 2017 |
| Received | Sep 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173175
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.