510(k) K080220 ยท DZI Drill, Bone, Powered
PIEZO ULTRASONIC DEVICE, MODEL ULTRASONIC BONE SURGERY; ULTRASONIC DEBRIDMENT DEVICE
| Applicant | Italia Medica S.R.L., Ormond Beach FL, US |
| Decision | Substantially Equivalent, Jul 28, 2008 |
| Received | Jan 29, 2008 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K080220
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.