ClearanceBrief
510(k) K103237 ยท NKB Thoracolumbosacral Pedicle Screw System

LANX SPINAL SYSTEM

ApplicantLanx, Inc., Broomfield CO, US
DecisionSubstantially Equivalent, Mar 25, 2011
ReceivedNov 2, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K103237

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.