ClearanceBrief
510(k) K001470 ยท KWP Appliance, Fixation, Spinal Interlaminal

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ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Aug 4, 2000
ReceivedMay 11, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001470

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.