510(k) K210146 ยท HWC Screw, Fixation, Bone
Cannulated Compression Device System
| Applicant | Orthopedic Designs North America, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Apr 13, 2022 |
| Received | Jan 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210146
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.