ClearanceBrief
510(k) K120760 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

LDR SPINE SPINETUNE TL SPINAL SYSTEM

ApplicantLdr Spine USA, Inc., Austin TX, US
DecisionSubstantially Equivalent, Jun 27, 2012
ReceivedMar 13, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120760

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.