ClearanceBrief
510(k) K072436 ยท MNI Orthosis, Spinal Pedicle Fixation

MEGA SPINE SYSTEM

ApplicantBk Meditech, Co., Ltd., Laguna Hills CA, US
DecisionSubstantially Equivalent, Nov 1, 2007
ReceivedAug 30, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072436

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.