510(k) K181610 ยท HWC Screw, Fixation, Bone
ActivOrtho Nitinol Compression Screw System
| Applicant | Activortho, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 12, 2019 |
| Received | Jun 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181610
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.