510(k) K162391 · HRS Plate, Fixation, Bone
AlignMATE Lapidus Arthrodesis System
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Feb 21, 2017 |
| Received | Aug 26, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162391
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.