510(k) K160652 ยท OUR Sacroiliac Joint Fixation
iFUSE Implant System
| Applicant | SI-BONE, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Jun 3, 2016 |
| Received | Mar 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160652
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.