510(k) K013739 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
MODIFICATION TO EBI XFIX DFS SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Dec 13, 2001 |
| Received | Nov 13, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013739
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.