510(k) K153631 ยท NKG Posterior Cervical Screw System
Zimmer Virage OCT Spinal Fixation System
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 16, 2016 |
| Received | Dec 18, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K153631
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.