ClearanceBrief
510(k) K102265 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM

ApplicantLdr Spine USA, Austin TX, US
DecisionSubstantially Equivalent, Sep 29, 2010
ReceivedAug 10, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K102265

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.