510(k) K152211 ยท NKG Posterior Cervical Screw System
PCT System
| Applicant | Centinel Spine, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, Dec 1, 2015 |
| Received | Aug 7, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152211
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.