ClearanceBrief
510(k) K121940 ยท NKB Thoracolumbosacral Pedicle Screw System

LANX SPINAL FIXATION SYSTEM

ApplicantLanx, Inc., Broomfield CO, US
DecisionSubstantially Equivalent, Aug 2, 2012
ReceivedJul 2, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121940

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.