510(k) K172886 ยท HRS Plate, Fixation, Bone
Breakaway Screw System
| Applicant | Paragon 28, Englewood CO, US |
| Decision | Substantially Equivalent, Dec 20, 2017 |
| Received | Sep 21, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172886
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.