510(k) K060270 ยท DZI Drill, Bone, Powered
MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Apr 10, 2006 |
| Received | Feb 1, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060270
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.