ClearanceBrief
510(k) K021039 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

BOWTI ANTERIOR BUTTRESS STAPLE SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Dec 11, 2002
ReceivedApr 1, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021039

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.