510(k) K031401 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
FIXION DYNAMIC HIP SCREW SYSTEM (FIXION DHS)
| Applicant | Disco-O-Tech Medical Technologies, Ltd., Herzlia, IL |
| Decision | Substantially Equivalent, Aug 6, 2003 |
| Received | May 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031401
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.