510(k) K172104 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Ozark(tm) Cervical Plate System
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Aug 23, 2017 |
| Received | Jul 12, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172104
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.