ClearanceBrief
510(k) K896740 ยท KWP Appliance, Fixation, Spinal Interlaminal

AXIAL AND OFFSET CROSSLINK PLATES

ApplicantDanek Medical, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Feb 26, 1990
ReceivedNov 30, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896740

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.