510(k) K161637 ยท NKG Posterior Cervical Screw System
Poseidon OCT Spinal Fixation System
| Applicant | Medyssey USA, Inc., Elk Grove Village IL, US |
| Decision | Substantially Equivalent, Jan 5, 2017 |
| Received | Jun 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161637
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.