ClearanceBrief
510(k) K993030 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

MODIFICATION TO ISOLA SPINAL SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Dec 29, 1999
ReceivedSep 7, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993030

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.