ClearanceBrief
510(k) K921056 ยท KWP Appliance, Fixation, Spinal Interlaminal

COTREL - DUBOUSSET SPINE IMPLANTS

ApplicantBuckman Co., Inc., Concord CA, US
DecisionSubstantially Equivalent, Jun 24, 1993
ReceivedMar 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921056

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.