510(k) K220658 ยท NKG Posterior Cervical Screw System
COSY Cervicothoracic Occipital Rod-Screw System
| Applicant | Signus Medizintechnik GmbH, Alzenau, DE |
| Decision | Substantially Equivalent, Nov 18, 2022 |
| Received | Mar 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220658
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.