ClearanceBrief
510(k) K002371 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM

ApplicantSpineology, Inc., Stillwater MN, US
DecisionSubstantially Equivalent, Sep 15, 2000
ReceivedJul 27, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K002371

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.