510(k) K071395 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
BIOMET VISION FOOTRING SYSTEM
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 9, 2007 |
| Received | May 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071395
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.