510(k) K001760 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
RADIOLUCENT COLLES FRACTURE KIT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 31, 2000 |
| Received | Jun 9, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K001760
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.