510(k) K151031 ยท NKG Posterior Cervical Screw System
Virage OCT Spinal Fixation System
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 24, 2015 |
| Received | Apr 17, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151031
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.