ClearanceBrief
510(k) K121103 ยท NKB Thoracolumbosacral Pedicle Screw System

LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S

ApplicantLdr Spine USA, Inc., Austin TX, US
DecisionSubstantially Equivalent, Aug 24, 2012
ReceivedApr 11, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121103

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.