510(k) K172594 · NKG Posterior Cervical Screw System
Proficient® Posterior Cervical Spine System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Aug 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172594
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.