510(k) K181350 ยท NKG Posterior Cervical Screw System
ASTRA-OCT Spine System
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, Jul 6, 2018 |
| Received | May 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181350
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.