ClearanceBrief
510(k) K001844 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION TO CENTAUR SPINAL SYSTEM

ApplicantHowmedica Osteonics Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Jul 19, 2000
ReceivedJun 19, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001844

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.