ClearanceBrief
510(k) K790404 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

DTT SYSTEM

ApplicantDepuy, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 21, 1979
ReceivedFeb 26, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790404

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.