510(k) K082906 ยท HWC Screw, Fixation, Bone
UNITY BETA ANCHOR SYSTEM
| Applicant | Bonutti Research, Inc., Effingham IL, US |
| Decision | Substantially Equivalent, Oct 30, 2008 |
| Received | Sep 30, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082906
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.