510(k) K003240 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
BIOMET EXTERNAL WRIST PLATE
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 29, 2000 |
| Received | Oct 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003240
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.