ClearanceBrief
510(k) K031888 ยท MNI Orthosis, Spinal Pedicle Fixation

MODIFICATION TO CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Jun 27, 2003
ReceivedJun 18, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031888

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.