510(k) K030372 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Mar 6, 2003 |
| Received | Feb 4, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030372
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.