510(k) K223708 ยท OUR Sacroiliac Joint Fixation
Entasis 3D Dual-Lead Sacroiliac Implant System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 21, 2023 |
| Received | Dec 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223708
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.