510(k) K170693 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
Phantom Small Bone Intramedullary Nail System
| Applicant | Paragon 28, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jun 19, 2017 |
| Received | Mar 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170693
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.