510(k) K162300 · NKG Posterior Cervical Screw System
Reform® POCT System
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Nov 22, 2016 |
| Received | Aug 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162300
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.