ClearanceBrief
510(k) K990603 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM

ApplicantDanek Medical, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Mar 10, 1999
ReceivedFeb 23, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K990603

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.