510(k) K172139 ยท NKG Posterior Cervical Screw System
Streamline OCT Occipito-Cervico-Thoracic System
| Applicant | Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.), Marquette MI, US |
| Decision | Substantially Equivalent, Aug 18, 2017 |
| Received | Jul 17, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172139
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.