510(k) K033112 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
WRISTJACK ORIF SYSTEM, WRISTJACK ORIF SYSTEM, NON-STERILE, MODELS CFD-347, CFD-347-NS
| Applicant | Hand Biomechanics Lab, Inc., Sacramento CA, US |
| Decision | Substantially Equivalent, Nov 5, 2003 |
| Received | Sep 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033112
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.