ClearanceBrief
510(k) K992110 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

PREMIER ANTERIOR CERVICAL PLATE SYSTEM

ApplicantSofamor Danek USA, Memphis TN, US
DecisionSubstantially Equivalent, Sep 14, 1999
ReceivedJun 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992110

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.