ClearanceBrief
510(k) K020650 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM

ApplicantHowmedica Osteonics Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Mar 29, 2002
ReceivedFeb 28, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020650

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.