510(k) K080761 ยท DZI Drill, Bone, Powered
BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES
| Applicant | Bonart Co., Ltd., Walnut CA, US |
| Decision | Substantially Equivalent, Aug 25, 2008 |
| Received | Mar 18, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080761
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.