510(k) K172275 · NKB Thoracolumbosacral Pedicle Screw System
Vitality® Spinal Fixation System, Vitality®+ Power Instrument System
| Applicant | Zimmer Biomet Spine, Inc., Westminister CO, US |
| Decision | Substantially Equivalent, Sep 27, 2017 |
| Received | Jul 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172275
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.