510(k) K203319 · NKG Posterior Cervical Screw System
SYMPHONY OCT System
| Applicant | Medos International SARL, Le Locle, CH |
| Decision | Substantially Equivalent, Feb 5, 2021 |
| Received | Nov 12, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203319
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.