510(k) K930836 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
HOWMEDICA(R) MONO-TUBE(TM) EXTERNAL FIXATOR SYSTEM
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Jan 18, 1995 |
| Received | Feb 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930836
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.