510(k) K233078 ยท NKG Posterior Cervical Screw System
Posterior Cervical Spine System
| Applicant | Double Medical Technology, Inc., Xiamen, CN |
| Decision | Substantially Equivalent, Nov 22, 2023 |
| Received | Sep 25, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233078
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.