510(k) K191344 · HRS Plate, Fixation, Bone
Arthrex Mini Comprehensive Fixation System 2.0mm & 2.4mm Module
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 3, 2019 |
| Received | May 20, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191344
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.