510(k) K203832 · JDR Staple, Fixation, Bone
FuseForce Flex Dynamic Compression System
| Applicant | Wright Medical, Memphis TN, US |
| Decision | Substantially Equivalent, May 7, 2021 |
| Received | Dec 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203832
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 10, 2022 | Wright Medical Technology, Inc. EasyFuse Dynamic Compression System Instrument Pack Terminated |
JDR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.