ClearanceBrief
510(k) K021979 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SMISSON STABILIZATION SYSTEM

ApplicantSmisson-Cartledge, Irvine CA, US
DecisionSubstantially Equivalent, Jun 27, 2003
ReceivedJun 17, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021979

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.