510(k) K123850 ยท OUR Sacroiliac Joint Fixation
IFUSE IMPLANT SYSTEM
| Applicant | SI-BONE, Inc., Hillsborough CA, US |
| Decision | Substantially Equivalent, Apr 1, 2013 |
| Received | Dec 14, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123850
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.