510(k) K233366 ยท NKG Posterior Cervical Screw System
SYMPHONY OCT System
| Applicant | Medos International SARL, Le Locle, CH |
| Decision | Substantially Equivalent, Nov 9, 2023 |
| Received | Oct 2, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233366
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.