ClearanceBrief
510(k) K001864 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SYNTHES CERVIFIX SYSTEM

ApplicantSynthes Spine, Paoli PA, US
DecisionSubstantially Equivalent, Jul 20, 2000
ReceivedJun 20, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001864

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.