510(k) K190751 ยท NKG Posterior Cervical Screw System
Connector System
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, May 22, 2019 |
| Received | Mar 25, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190751
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.