510(k) K201850 ยท HWC Screw, Fixation, Bone
Vector Hammertoe Correction System
| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Aug 4, 2020 |
| Received | Jul 6, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K201850
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.