ClearanceBrief
510(k) K982875 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION TO ZPLATE-ATL ANTERIOR FIXATION SYSTEM

ApplicantDanek Medical, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Jan 19, 1999
ReceivedAug 14, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K982875

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.