ClearanceBrief
510(k) K022908 ยท MNI Orthosis, Spinal Pedicle Fixation

POSTERIOR CABLE SCREW

ApplicantPioneer Surgical Technology, Marquette MI, US
DecisionSubstantially Equivalent, Jan 22, 2004
ReceivedSep 3, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022908

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.