510(k) K192014 · NKG Posterior Cervical Screw System
SYPMHONY OCT System
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Jan 24, 2020 |
| Received | Jul 29, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192014
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.