510(k) K863343 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
SUPERFIXATION(TM)
| Applicant | Orthopaedic Device Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Sep 15, 1986 |
| Received | Aug 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863343
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.