510(k) K122733 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
V2F ANTERIOR FIXATION SYSTEM
| Applicant | Zimmer Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Dec 7, 2012 |
| Received | Sep 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122733
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.