510(k) K002923 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
DYNAMIC JOINT DISTRACTOR II EXTERNAL FIXATION SYSTEM
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Dec 18, 2000 |
| Received | Sep 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002923
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.