ClearanceBrief
510(k) K002980 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION TO EBI ANTERIOR CERVICAL PLATE SYSTEM

ApplicantEbi, L.P., Parsippany NJ, US
DecisionSubstantially Equivalent, Oct 23, 2000
ReceivedSep 25, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002980

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.