ClearanceBrief
510(k) K081296 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

PREFERENCE PEDICLE SCREW SYSTEM

ApplicantUs Spine, Apple Valley MN, US
DecisionSubstantially Equivalent, Jun 6, 2008
ReceivedMay 7, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081296

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.