510(k) K220195 · OUR Sacroiliac Joint Fixation
iFuse Bedrock Granite Implant System
| Applicant | SI-BONE, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, May 26, 2022 |
| Received | Jan 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220195
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.