ClearanceBrief
510(k) K002505 ยท KWP Appliance, Fixation, Spinal Interlaminal

XIA SPINE SYSTEM

ApplicantHowmedica Osteonics Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Oct 5, 2000
ReceivedAug 15, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002505

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.