510(k) K032607 ยท DZI Drill, Bone, Powered
POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Nov 10, 2003 |
| Received | Aug 25, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032607
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.