510(k) K172279 ยท NKG Posterior Cervical Screw System
PMT Posterior Fixation System
| Applicant | Providence Medical Technology, Inc., Walnut Creek CA, US |
| Decision | Substantially Equivalent, Sep 20, 2017 |
| Received | Jul 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172279
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.