510(k) K232897 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Arthrex Small External Fixation System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 18, 2023 |
| Received | Sep 18, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232897
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.