ClearanceBrief
510(k) K984348 ยท MNI Orthosis, Spinal Pedicle Fixation

TIMX LOW BACK SYSTEM

ApplicantDepuy Motech Acromed, Cleveland OH, US
DecisionSubstantially Equivalent, Jan 20, 1999
ReceivedDec 4, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984348

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.