ClearanceBrief
510(k) K093170 ยท MNI Orthosis, Spinal Pedicle Fixation

ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

ApplicantSpineart, Geneva, CH
DecisionSubstantially Equivalent, Nov 4, 2009
ReceivedOct 7, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093170

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.