510(k) K181440 · NKG Posterior Cervical Screw System
Proficient® Posterior Cervical Spine System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jul 30, 2018 |
| Received | Jun 1, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181440
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.