ClearanceBrief
510(k) K030840 ยท MNI Orthosis, Spinal Pedicle Fixation

MODIFICATION TO HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Inc., Memphis TN, US
DecisionSubstantially Equivalent, May 15, 2003
ReceivedMar 17, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030840

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.