510(k) K202833 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Sequel External Fixation Device
| Applicant | Sequel Medical, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Jan 19, 2021 |
| Received | Sep 25, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202833
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.