ClearanceBrief
510(k) K921256 ยท KWP Appliance, Fixation, Spinal Interlaminal

LUQUE V SPINAL SYSTEM

ApplicantSofamor Danek Mfg., Inc., Memphis TN, US
DecisionSubstantially Equivalent for Some Indications, May 18, 1993
ReceivedMar 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921256

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.