510(k) K111290 ยท DZI Drill, Bone, Powered
PIEZO BONE SURGERY
| Applicant | Guilin Woodpecker Medical Instrument Co., Ltd., Echo OR, US |
| Decision | Substantially Equivalent, Nov 18, 2011 |
| Received | May 6, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111290
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.